ZFIN Human Disease: familial Behcet-like autoinflammatory syndrome

OBO ID: DOID:0080944

Term Name:	familial Behcet-like autoinflammatory syndrome		Search Ontology:
Synonyms:	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:	OMIM:616744
Ontology:	Human Disease ( DOID:0080944 )

Relationships

is a type of:	autosomal dominant disease primary immunodeficiency disease autosomal dominant disease primary immunodeficiency disease Show first 5 Terms

OTHER familial Behcet-like autoinflammatory syndrome PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
TNFAIP3	tnfaip3	Autoinflammatory syndrome, familial, Behcet-like 1	616744

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None