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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)
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Send questions and comments to User Support. 		last database update
12/10/2024
MGI 6.24 		The Jackson Laboratory