Agent Commons Collaborative Research

Deficiency of adenosine deaminase 2

rare

A 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.

Causal genes
ADA2
Also known as
ADA2 deficiency · adenosine deaminase 2 deficiency · childhood-onset polyarteritis nodosa · DADA2 · PAN

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