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gptkbp:instanceOf
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gptkb:disease
genetic disorder
bleeding disorder
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gptkbp:affects
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blood clotting
both males and females
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gptkbp:causedBy
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deficiency of von Willebrand factor
dysfunction of von Willebrand factor
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gptkbp:complication
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gptkb:anemia
severe bleeding
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gptkbp:diagnosedBy
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gptkb:ristocetin_cofactor_activity_test
gptkb:von_Willebrand_factor_antigen_test
blood tests
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gptkbp:firstDescribed
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1926
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gptkbp:frequency
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1 in 100 to 1 in 1000 people
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gptkbp:hasType
|
Type 1
Type 2
Type 3
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|
https://www.w3.org/2000/01/rdf-schema#label
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Von Willebrand disease
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gptkbp:ICD-10_code
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gptkb:D68.0
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gptkbp:inheritance
|
autosomal dominant
autosomal recessive
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gptkbp:namedAfter
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gptkb:Erik_Adolf_von_Willebrand
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gptkbp:OMIM
|
193400
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gptkbp:prevalence
|
most common inherited bleeding disorder
|
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gptkbp:riskFactor
|
family history
genetic disorder
|
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gptkbp:symptom
|
bleeding gums
easy bruising
prolonged bleeding
frequent nosebleeds
heavy menstrual bleeding
|
|
gptkbp:treatment
|
gptkb:desmopressin
gptkb:antifibrinolytic_drugs
gptkb:von_Willebrand_factor_concentrates
|
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gptkbp:bfsParent
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gptkb:D68.0
gptkb:Platelet_plug
gptkb:Von_Willebrand_factor
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gptkbp:bfsLayer
|
6
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