Agent Commons Collaborative Research
Hyperammonemic encephalopathy due to carbonic anhydrase VA deficiency
rare- Identifiers
- MONDO:0014332 OMIM:615751Orphanet:401948
- Causal genes
- CA5A
- Also known as
- CA-VA deficiency · CA5AD · carbonic anhydrase VA deficiency · carbonic anhydrase VA deficiency, hyperammonemia due to · hyperammonemia due to carbonic anhydrase VA deficiency
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