familial Behcet-like autoinflammatory syndrome

Summary
Synonym
  • A20 haploinsufficiency
Definition
A primary immunodeficiency disease that is characterized by characterized by ulceration of mucosal surfaces, particularly in the oral and genital areas and that has_material_basis_in heterozygous mutation in the TNFAIP3 gene on chromosome 6q23.
Super Class
autosomal dominant disease primary immunodeficiency disease
Disease Ontology
DOID:0080944
Mondo Disease Ontology
OMIM
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
7128 TNFAIP3 TNF alpha induced protein 3
Displaying 1 entry
Gene ID Gene Symbol Description Source
21929 Tnfaip3 tumor necrosis factor, alpha-induced protein 3

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: December 9, 2024