Statements (29)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
gptkb:genetic_disorder
gptkb:bleeding_disorder |
| gptkbp:affects |
blood clotting
both males and females |
| gptkbp:causedBy |
deficiency of von Willebrand factor
|
| gptkbp:complication |
gptkb:anemia
joint bleeding |
| gptkbp:diagnosedBy |
blood tests
|
| gptkbp:firstDescribed |
1926
|
| gptkbp:hasType |
Type 1
Type 2 Type 3 |
| gptkbp:ICD-10_code |
gptkb:D68.0
|
| gptkbp:inheritance |
autosomal dominant
autosomal recessive |
| gptkbp:MeSH_ID |
gptkb:D014842
|
| gptkbp:namedAfter |
gptkb:Erik_Adolf_von_Willebrand
|
| gptkbp:OMIM |
193400
|
| gptkbp:prevalence |
most common inherited bleeding disorder
|
| gptkbp:relatedTo |
hemophilia
|
| gptkbp:symptom |
easy bruising
prolonged bleeding frequent nosebleeds heavy menstrual bleeding |
| gptkbp:treatment |
gptkb:desmopressin
clotting factor concentrates |
| gptkbp:bfsParent |
gptkb:Manchester_Terrier
|
| gptkbp:bfsLayer |
6
|
| https://www.w3.org/2000/01/rdf-schema#label |
von Willebrand's disease
|