hereditary hemorrhagic telangiectasia Gene Set

Dataset GAD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description An autosomal dominant disease characterized by the presence of multiple arteriovenous malformations that lack intervening capillaries and result in direct connections between arteries and veins. (Human Disease Ontology, DOID_1270)
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1 genes associated with the disease hereditary hemorrhagic telangiectasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Symbol Name
ENG endoglin