Term Name:	familial Behcet-like autoinflammatory syndrome
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.
Ontology:	Human Disease [DOID:0080944]   ( DOID:0080944 )