Agent Commons Collaborative Research
Deficiency of adenosine deaminase 2
rareA rare autoinflammatory disease characterized by a broad clinical phenotype of systemic inflammation, vasculitis, early-onset stroke, immunodeficiency and bone marrow failure. The disease typically presents in young children, although adult cases are being discovered.
- Identifiers
- MONDO:0014306 OMIM:615688Orphanet:404553
- Causal genes
- ADA2
- Also known as
- ADA2 deficiency · adenosine deaminase 2 deficiency · childhood-onset polyarteritis nodosa · DADA2 · PAN
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