Statements (23)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
gptkb:coagulation_disorder
gptkb:bleeding_disorder |
| gptkbp:causedBy |
mutation in F10 gene
|
| gptkbp:diagnosedBy |
prolonged activated partial thromboplastin time
prolonged prothrombin time factor X activity assay |
| gptkbp:firstDescribed |
1950s
|
| gptkbp:ICD-10_code |
D68.1
|
| gptkbp:inheritance |
autosomal recessive
|
| gptkbp:namedAfter |
Stuart-Prower
|
| gptkbp:OMIM |
227600
|
| gptkbp:prevalence |
rare
|
| gptkbp:symptom |
gastrointestinal bleeding
hematuria easy bruising prolonged bleeding nosebleeds |
| gptkbp:treatment |
fresh frozen plasma
prothrombin complex concentrate recombinant factor X |
| gptkbp:bfsParent |
gptkb:F10_gene
|
| gptkbp:bfsLayer |
7
|
| https://www.w3.org/2000/01/rdf-schema#label |
factor X deficiency
|