Autoinflammatory Syndrome, Familial, Behcet-Like M35.2

Last updated on: 09.05.2022

Definition
This section has been translated automatically.

Behcet-like familial autoinflammatory syndrome is a rare autosomal dominant monogenic autoinflammatory syndrome caused by a heterozygous mutation in the TNFAIP3 gene (191163) on chromosome 6q23.

Last updated on: 09.05.2022

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