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Summary Literature (0)
DOID:0060574 - von Willebrand's disease 2

Disease Ontology Definition:A von Willebrand's disease characterized by qualitative but not quantitative abnormalities of the VWF protein that has_material_basis_in mutation in the VWF gene which maps to chromosome 12p13.

Synonyms: von Willebrand disease type 2, von Willebrand disease type II, VWD2, VWD type 2

Xenbase Genes : vwf

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0013304 - von Willebrand disease 2


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)