Search Ontology:
Human Disease
familial Behcet-like autoinflammatory syndrome
- Term ID
- DOID:0080944
- Synonyms
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- 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. https://pubmed.ncbi.nlm.nih.gov/26642243/
- References
- Ontology
- Human Disease ( DOID:0080944 )
- is a type of
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Other Pages
Genes Involved
Zebrafish Models