Term Name: familial Behcet-like autoinflammatory syndrome
Synonyms: A20 haploinsufficiency
Definition: An autoinflammatory 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 )

Relationships
is a type of: autoinflammatory disease autosomal dominant disease