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Human Disease

familial Behcet-like autoinflammatory syndrome

Term ID
DOID:0080944
Synonyms
  • 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. https://pubmed.ncbi.nlm.nih.gov/26642243/
References
Ontology
Human Disease   ( DOID:0080944 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models