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Disease Ontology Browser
von Willebrand's disease 2 (DOID:0060574)
Alliance: disease page
Synonyms: von Willebrand disease type 2; von Willebrand disease type II; VWD2; VWD type 2
Alt IDs: OMIM:613554, ICD10CM:D68.02, MESH:D056728, ORDO:166081, UMLS_CUI:C1264040
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.

Disease References using Mouse Models (1)
Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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Send questions and comments to User Support. 		last database update
04/30/2024
MGI 6.23 		The Jackson Laboratory