5C50.21 Urocanic aciduria
International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2024-01
This is an autosomal recessive metabolic disorder caused by a deficiency of the enzyme urocanase. It is a secondary disorder of histidine metabolism.
postcoordination
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Has manifestation - multiple selections are allowed
synonyms
- Urocanic aciduria
- Encephalopathy due to urocanase deficiency
- Urocanate hydratase deficiency
- Urocanase deficiency
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