Symbol Name ID |
Vwf
Von Willebrand factor MGI:98941 |
Darker colors indicate more annotations |
Human Phenotypes | Gastrointestinal hemorrhage |
Hematemesis |
Joint hemorrhage |
Bruising susceptibility |
Purpura |
Petechiae |
Spontaneous hematomas |
Mitral valve prolapse |
Peripheral arterial stenosis |
Abnormal cerebral vascular morphology |
Ischemic stroke |
Transient ischemic attack |
Gastrointestinal angiodysplasia |
Aortic valve stenosis |
Raynaud phenomenon |
Cerebral ischemia |
Pulmonary arterial hypertension |
Myocardial infarction |
Syncope |
Splenomegaly |
Erythema |
Disease(s) Associated with VWF | |||||||||||||||||||||
Behcet's disease | |||||||||||||||||||||
Bernard-Soulier syndrome | |||||||||||||||||||||
essential thrombocythemia | |||||||||||||||||||||
von Willebrand's disease 1 | |||||||||||||||||||||
von Willebrand's disease 2 | |||||||||||||||||||||
von Willebrand's disease 3 |
Mouse Phenotypes | internal hemorrhage |
decreased myocardial infarct size |
impaired blood-brain barrier function |
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Availability | Mouse Genotype | |||
Vwftm1Wgr/Vwftm1Wgr |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO) |
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last database update 04/30/2024 MGI 6.23 |
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