Urocanic aciduria (Q39998): Difference between revisions
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CID11:5C50.21 | |||
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Revision as of 05:38, 13 August 2026
This is an autosomal recessive metabolic disorder caused by a deficiency of the enzyme urocanase. It is a secondary disorder of histidine metabolism.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | 5C50.21 |
||
| English | Urocanic aciduria |
This is an autosomal recessive metabolic disorder caused by a deficiency of the enzyme urocanase. It is a secondary disorder of histidine metabolism. |
Statements
CID11:5C50.21
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