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DOID:0111054 - von Willebrand's disease 3
Disease Ontology 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.
Synonyms: von Willebrand disease type 3, von Willebrand disease type III, VWD3, VWD type 3
Xenbase Genes
:
vwf
| MONDO:0010191 - aortic system |
| MIM:277480 - VON WILLEBRAND DISEASE, TYPE 3; VWD3 |
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)