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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: VWD type 2, VWD2, von Willebrand disease type 2, von Willebrand disease type II,
Echinobase Genes :
MIM:613554 - von willebrand disease, type 2; vwd2 |
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)