FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term familial Behcet-like autoinflammatory syndrome ID (Ontology) DOID:0080944 (Human Disease)
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.
Also Known As "A20 haploinsufficiency"
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 Genes
 familial Behcet-like autoinflammatory syndrome       1
 for disease ribbon | familial Behcet-like autoinflammatory syndrome       1
 model of | familial Behcet-like autoinflammatory syndrome       1
Spanning Tree (Parents/Children)
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autosomal genetic disease
 |__autosomal dominant disease____
primary immunodeficiency disease  |
 |__autoinflammatory disease______|
                                  familial Behcet-like autoinflammatory syndrome  1 rec.
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Is a autosomal dominant disease
autoinflammatory disease
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Synonyms
  • "A20 haploinsufficiency" EXACT
Secondary IDs
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MIM:616744