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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, 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.


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Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
07/31/2018
MGI 6.12
The Jackson Laboratory