moyamoya phenomenon Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
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 http://compbio.charite.de/hpoweb/showterm?id=HP:0011834
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Genes

2 genes associated with the moyamoya phenomenon phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ACTA2 actin, alpha 2, smooth muscle, aorta
PCNT pericentrin