Moyamoya Phenomenon Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A noninflammatory, progressive occlusion of the intracranial carotid arteries owing to the formation of netlike collateral arteries arising from the circle of Willis. (Human Phenotype Ontology, HP_0011834)
External Link https://www.disgenet.org/browser/0/1/0/C4023169
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Genes

10 genes associated with the disease Moyamoya Phenomenon in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ACTA2 actin, alpha 2, smooth muscle, aorta
ADAR adenosine deaminase, RNA-specific
GUCY1A3 guanylate cyclase 1, soluble, alpha 3
IFIH1 interferon induced with helicase C domain 1
PCNT pericentrin
RNASEH2A ribonuclease H2, subunit A
RNASEH2B ribonuclease H2, subunit B
RNASEH2C ribonuclease H2, subunit C
SAMHD1 SAM domain and HD domain 1
TREX1 three prime repair exonuclease 1