moyamoya disease Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A cerebral arterial disease characterized by constriction of certain arteries at the base of the brain. Blood flow is blocked by the constriction and also by blood clots. (Human Disease Ontology, DOID_13099)
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Genes

1 genes associated with the moyamoya disease phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
MYMY1 moyamoya disease 1