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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,
Xenbase Genes : vwf
MONDO:0008668 - von Willebrand disease 1 |
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
von Willebrand's disease (is_a)