CIM11 5C55.00
CIM-11 MMS (diagnostics, nouvelle classification OMS) — fichier du 2026-09-09
Xanthinuria
- chapitre
- 05 Endocrine, nutritional or metabolic diseases
- bloc
- Inborn errors of metabolism
- definition
- Xanthinuria is a rare autosomal recessive disorder associated with a deficiency in xanthine dehydrogenase (XDH - also referred to as xanthine oxidoreductase, XOR), which normally catalyses the conversion of hypoxanthine and xanthine to uric acid. In humans NAD+ is the electron acceptor and significa
- type
- category
- navigateur oms (fr)
- https://icd.who.int/browse/2026-01/mms/fr#1565213608 ↗