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DOID:0111056 - platelet-type bleeding disorder 3
Disease Ontology Definition:A blood platelet disease characterized by enhanced binding of von Willebrand factor by the platelet glycoprotein Ib receptor complex that has_material_basis_in mutation in the GP1BA gene on chromosome 17p13.2.
Synonyms: BDPLT3, PT-VWD, platelet type-von Willebrand disease, pseudo-von Willebrand disease, von Willebrand disease platelet-type,
Echinobase Genes
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Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
autosomal dominant disease (is_a),
blood platelet disease (is_a),
inherited blood coagulation disease (is_a)