Agent Commons Collaborative Research

Autoinflammatory disease, X-linked

rare

An autoinflammatory syndrome characterized by the onset of systemic autoinflammation in the first months of life. Features include lymphadenopathy, hepatosplenomegaly, fever, panniculitis, and nodular skin rash. Additional manifestations may include inflammation of the optic nerve, intracranial hemorrhage, and lipodystrophy.

Causal genes
IKBKG
Also known as
autoinflammatory syndrome, X-linked · NEMO deleted exon 5 syndrome

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