Pseudo von Willebrand disease Gene Set

Dataset ClinVar Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description Platelet type Von Willebrand disease (PT-VWD) is a bleeding disorder characterized by mild to moderate mucocutaneous bleeding, which becomes more pronounced during pregnancy or following ingestion of drugs that have anti-platelet activity. PT-VWD is due to hyperresponsive platelets, resulting in thrombocytopenia. (Orphanet Rare Disease Ontology, Orphanet_52530)
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1 genes associated with the Pseudo von Willebrand disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Symbol Name
GP1BA glycoprotein Ib (platelet), alpha polypeptide