OBO ID: DOID:0080944 |
Term Name: | familial Behcet-like autoinflammatory syndrome | Search Ontology: | |
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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/ | ||
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Ontology: | Human Disease ( DOID:0080944 ) |
OTHER familial Behcet-like autoinflammatory syndrome PAGES
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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