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Summary Literature (0)
DOID:0060573 - von Willebrand's disease 1

Disease Ontology Definition:A von Willebrand's disease characterized by quantitative partial deficiency of circulating VWF that has_material_basis_in heterozygous mutation in the VWF gene on chromosome 12p13.

Synonyms: von Willebrand disease type 1, von Willebrand disease type I, VWD1, VWD type 1

Xenbase Genes : vwf

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0008668 - von Willebrand disease 1

MIM:
MIM:193400 - VON WILLEBRAND DISEASE, TYPE 1; VWD1

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): von Willebrand's disease (is_a)