5C60

ICD-11 MMS 2026-01

Disorders of amino acid absorption or transport

Description

Any condition caused by deficiencies in amino acid absorption and transport.

Excludes

  • 5C50.3 – Disorders of tryptophan metabolism

Exclusions from above levels

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

  • 5C60.0 – Oculocerebrorenal syndrome
  • 5C60.1 – Cystinosis
  • 5C60.2 – Cystinuria
  • 5C60.Y – Other specified disorders of amino acid absorption or transport
  • 5C60.Z – Disorders of amino acid absorption or transport, unspecified

Foundation children elsewhere

Sibling codes

  • 5C61 – Disorders of carbohydrate absorption or transport
  • 5C62 – Disorders of lipid absorption or transport
  • 5C63 – Disorders of vitamin or non-protein cofactor 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 amino acid absorption or transport – http://id.who.int/icd/entity/1631611896

Part of: 05: Endocrine, nutritional or metabolic diseases