CIM11 5C50.21
CIM-11 MMS (diagnostics, nouvelle classification OMS) — fichier du 2026-09-09
Urocanic aciduria
- chapitre
- 05 Endocrine, nutritional or metabolic diseases
- bloc
- Inborn errors of metabolism
- definition
- This is an autosomal recessive metabolic disorder caused by a deficiency of the enzyme urocanase. It is a secondary disorder of histidine metabolism.
- type
- category
- navigateur oms (fr)
- https://icd.who.int/browse/2026-01/mms/fr#61773927 ↗