Statements (56)
| Predicate | Object |
|---|---|
| gptkbp:instance_of |
gptkb:Genetics
|
| gptkbp:affects |
blood clotting
|
| gptkbp:associated_with |
gptkb:Fuchsia
|
| gptkbp:can_cause |
gptkb:anemia
fatigue pain |
| gptkbp:can_lead_to |
gastrointestinal bleeding
joint problems heavy menstrual bleeding |
| gptkbp:caused_by |
deficiency of von Willebrand factor
|
| gptkbp:diagnosis |
gptkb:hemophilia_A
blood tests thrombocytopenia other bleeding disorders |
| gptkbp:difficulty_levels |
gptkb:Type_3
|
| gptkbp:first_described_by |
gptkb:Erik_von_Willebrand
|
| gptkbp:has_achieved |
gptkb:surgery
injury pregnancy |
| https://www.w3.org/2000/01/rdf-schema#label |
von Willebrand disease
|
| gptkbp:inherits_from |
autosomal dominant
|
| gptkbp:is |
gptkb:hemophilia_B
acquired bleeding disorder thrombotic disorder |
| gptkbp:is_common_in |
both genders
all ethnic groups |
| gptkbp:is_less_severe_in |
Type 1
Type 2 |
| gptkbp:is_monitored_by |
treatment response
factor levels bleeding episodes |
| gptkbp:is_recognized_by |
genetic testing
ristocetin cofactor assay von Willebrand factor activity test |
| gptkbp:is_related_to |
gptkb:von_Willebrand_factor
coagulation cascade platelet function |
| gptkbp:is_studied_in |
clinical trials
|
| gptkbp:managed_by |
hematologist
|
| gptkbp:prevalence |
1% of the population
|
| gptkbp:screenings |
family history
clinical evaluation laboratory tests |
| gptkbp:symptoms |
easy bruising
excessive bleeding prolonged bleeding after injury |
| gptkbp:treatment |
platelet transfusions
desmopressin factor replacement therapy hormonal therapy antifibrinolytics |
| gptkbp:type_of |
gptkb:Type_3
Type 1 Type 2 |
| gptkbp:bfsParent |
gptkb:Dog
|
| gptkbp:bfsLayer |
4
|