Statements (10)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
gptkb:ICD-10
|
| gptkbp:codename |
gptkb:Von_Willebrand_disease
|
| gptkbp:describes |
Von Willebrand disease is a hereditary bleeding disorder caused by deficiency or dysfunction of von Willebrand factor.
|
| gptkbp:foundIn |
gptkb:ICD-10
|
| https://www.w3.org/2000/01/rdf-schema#label |
D68.0
|
| gptkbp:partOf |
gptkb:ICD-10_Chapter_III:_Diseases_of_the_blood_and_blood-forming_organs_and_certain_disorders_involving_the_immune_mechanism
|
| gptkbp:relatedTo |
bleeding disorders
|
| gptkbp:usedIn |
diagnosis
|
| gptkbp:bfsParent |
gptkb:von_Willebrand's_disease
|
| gptkbp:bfsLayer |
5
|