Human genes for familial Behcet-like autoinflammatory syndrome
Familial Behcet-like autoinflammatory syndrome [DOID:0080944]
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.
Synonyms: familial Behcet-like autoinflammatory syndrome, DOID:0080944, familial Behcetlike autoinflammatory syndrome, familial Behcet-like autoinflammatory disease, familial Behcet-like autoinflammatory disorder ...