behcet's disease Gene Set

Dataset GAD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A vasculitis that is characterized by an autoimmune mediated inflammation of the blood vessels throughout the body leading to ulcerations on the mouth and sometimes the genitals, notorious for causing hypopyon uveitis. (Human Disease Ontology, DOID_13241)
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22 genes associated with the disease behcet's disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Symbol Name
ACE angiotensin I converting enzyme
CCL2 chemokine (C-C motif) ligand 2
CTLA4 cytotoxic T-lymphocyte-associated protein 4
CXCR2 chemokine (C-X-C motif) receptor 2
CYP1A1 cytochrome P450, family 1, subfamily A, polypeptide 1
F2 coagulation factor II (thrombin)
F5 coagulation factor V (proaccelerin, labile factor)
HLA-A major histocompatibility complex, class I, A
HLA-B major histocompatibility complex, class I, B
HLA-C major histocompatibility complex, class I, C
IL1A interleukin 1, alpha
ITGA2 integrin, alpha 2 (CD49B, alpha 2 subunit of VLA-2 receptor)
MBL2 mannose-binding lectin (protein C) 2, soluble
MEFV Mediterranean fever
MICA MHC class I polypeptide-related sequence A
MICB MHC class I polypeptide-related sequence B
NOS3 nitric oxide synthase 3 (endothelial cell)
SOD2 superoxide dismutase 2, mitochondrial
TAP1 transporter 1, ATP-binding cassette, sub-family B (MDR/TAP)
TAP2 transporter 2, ATP-binding cassette, sub-family B (MDR/TAP)
TNF tumor necrosis factor
VEGFA vascular endothelial growth factor A