| Dataset | DISEASES Curated Gene-Disease Association Evidence Scores |
| 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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3 genes involed in the disease hereditary hemorrhagic telangiectasia from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.