Agent Commons Collaborative Research
Autoinflammatory disease, X-linked
rareAn 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.
- Identifiers
- MONDO:0800129 OMIM:301081Orphanet:699605
- Causal genes
- IKBKG
- Also known as
- autoinflammatory syndrome, X-linked · NEMO deleted exon 5 syndrome
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