5C60.2

ICD-11 MMS 2026-01

Cystinuria

Description

Cystinuria is a renal tubular aminoacid transport disorder characterised by recurrent formation of kidneys cystine stones.

Index terms

  • Cystinuria
  • CSNU - [cystinuria]
  • Cystinuria - lysinuria
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  • cystine disease
  • Cystinuria type A
  • Cystinuria type B

Exclusions from above levels

  • 5C50.3 – Disorders of tryptophan metabolism
  • 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

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

Foundation entity

Cystinuria – http://id.who.int/icd/entity/1237620397

Part of: 5C60: Disorders of amino acid absorption or transport › 05: Endocrine, nutritional or metabolic diseases