About   Help   FAQ
Disease Ontology Browser
von Willebrand's disease 3 (DOID:0111054)
Alliance: disease page
Synonyms: von Willebrand disease type 3; von Willebrand disease type III; VWD3; VWD type 3
Alt IDs: OMIM:277480, ICD10CM:D68.03, MESH:D056729, NCI:C85213, ORDO:166096, UMLS_CUI:C1264041
Definition: A von Willebrand's disease characterized by autosomal recessive inheritance of a severe quantitative defect or virtual absence of VWF in plasma, prolonged bleeding time, and more severe bleeding tendencies compared to the other types of von Willebrand disease that has_material_basis_in homozygous or compound heterozygous mutation in the VWF gene which maps to chromosome 12p13.

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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support. 		last database update
11/12/2024
MGI 6.24 		The Jackson Laboratory