5C63

ICD-11 MMS 2026-01

Disorders of vitamin or non-protein cofactor absorption or transport

Exclusions from above levels

  • 3A10.Z – Hereditary haemolytic anaemia due to enzyme deficiency
  • 5A71.01 – Congenital adrenal hyperplasia
  • 5A81.1 – 5-alpha-reductase deficiency
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  • 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

Child codes

  • 5C63.0 – Disorders of cobalamin metabolism or transport
  • 5C63.1 – Disorders of folate metabolism or transport
  • 5C63.2 – Disorders of vitamin D metabolism or transport
  • 5C63.Y – Other specified disorders of vitamin or non-protein cofactor absorption or transport
  • 5C63.Z – Disorders of vitamin or non-protein cofactor absorption or transport, unspecified

Foundation children elsewhere

  • 3B14.1 – Hereditary factor X deficiency
  • 3B14.2 – Combined deficiency of vitamin K-dependent clotting factors

Sibling codes

  • 5C60 – Disorders of amino acid absorption or transport
  • 5C61 – Disorders of carbohydrate absorption or transport
  • 5C62 – Disorders of lipid absorption or transport
  • 5C64 – Disorders of mineral absorption or transport
  • 5C6Y – Other specified disorders of metabolite absorption or transport
  • 5C6Z – Disorders of metabolite absorption or transport, unspecified

Foundation entity

Disorders of vitamin or non-protein cofactor absorption or transport – http://id.who.int/icd/entity/1112006621

Part of: 05: Endocrine, nutritional or metabolic diseases