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DO Term : familial Behcet-like autoinflammatory syndrome [DOID:0080944] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  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.
  • synonyms:
  • OMIM:616744,
  • A20 haploinsufficiency,
  • 616744
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Disease

Diseases --> Human genes

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Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

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Ontology Term --> Direct children

Ontology Term --> Direct parents





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