| 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 ) |