CIM11 5C50.10
CIM-11 MMS (diagnostics, nouvelle classification OMS) — fichier du 2026-09-09
Alkaptonuria
- chapitre
- 05 Endocrine, nutritional or metabolic diseases
- bloc
- Inborn errors of metabolism
- definition
- Alkaptonuria is characterised by the accumulation of homogentisic acid (HGA) and its oxidised product benzoquinone acetic acid (BQA), leading to a darkening of the urine when it is left exposed to air, grey-blue colouration of the eye sclerae and the ear helix (ochronosis), and a disabling joint dis
- type
- category
- navigateur oms (fr)
- https://icd.who.int/browse/2026-01/mms/fr#1761652827 ↗