Von Willebrand's Disease

Alias:
Von Willebrand Disease
Von Willebrand Disorder
Hereditary Von Willebrand Disease
Vascular Pseudohemophilia
Factor Viii Deficiency with Vascular Defect
Minot-Von Willebrand-Jurgen Disease
Von Willebrand's Factor Deficiency
Von Willebrand's-Jurgens' Disease
Von Willebrand Factor Deficiency
Willebrand Jurgen Thrombopathy
Von Willebrand-Jrgens Disease
Von Willebrand Diseases
Vascular Haemophilia
Vascular Hemophilia
Angiohaemophilia a
Angiohaemophilia B
Pseudohaemophilia
Angiohaemophilia
Angiohemophilia
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Von Willebrand's Disease, also known as von willebrand disease, is related to von willebrand disease, type 2 and von willebrand disease, type 3. An important gene associated with Von Willebrand's Disease is VWF (Von Willebrand Factor), and among its related pathways/superpathways are Infectious disease and Response to elevated platelet cytosolic Ca2+. The drugs Arginine and Deamino Arginine Vasopressin have been mentioned in the context of this disorder. Affiliated tissues include bone marrow and bone, and related phenotypes are abnormality of thrombocytes and abnormal platelet function
Related ID:
MESH:D014842
ICD11:2112021600

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AR
AD
All ages
1-5/10000
23
175
181

Medical Symptom

#
Categorization
Description
HPO Frequency
Orphanet Frequency
HPO Source Accession
No data available

Gene & Mutation

#
Gene
Function
Score
Mutations
No data available

Related Drugs

Name
CAS Number
Status
Phase
No data available

Disease Model

Category
Name
MGI
Related Gene
Strain of Origin
Publications
No data available

References Literature

Title
PMID
Journal
Year
IF
No Data Found!
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