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Echinobase
Summary Literature (0)
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 :


OMIM:
MIM:193400 - von willebrand disease, type 1; vwd1

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)