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DOID:0060573 - von Willebrand's disease 1
Disease Ontology Definition:A von Willebrand's disease characterized by quantitative partial deficiency of circulating VWF that has material_basis_in heterozygous mutation in the VWF gene on chromosome 12p13.
Synonyms: VWD type 1, VWD1, von Willebrand disease type 1, von Willebrand disease type I,
Echinobase Genes :
MIM:193400 - von willebrand disease, type 1; vwd1 |
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)