Statements (23)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
gptkb:genetic_disorder
gptkb:coagulation_disorder gptkb:rare_disease |
| gptkbp:affects |
blood clotting
|
| gptkbp:alsoKnownAs |
gptkb:Factor_X_deficiency
|
| gptkbp:deficiencyCauses |
gptkb:coagulation_factor_X
|
| gptkbp:diagnosedBy |
coagulation tests
|
| gptkbp:firstDescribed |
1953
|
| gptkbp:ICD-10_code |
D68.1
|
| gptkbp:inheritance |
autosomal recessive
|
| gptkbp:mutationAssociatedWith |
gptkb:F10_gene
|
| gptkbp:namedAfter |
gptkb:Edmund_Stuart
R. R. Prower |
| gptkbp:OMIM |
227600
|
| gptkbp:prevalence |
very rare
|
| gptkbp:symptom |
easy bruising
prolonged bleeding nosebleeds |
| gptkbp:treatment |
fresh frozen plasma
prothrombin complex concentrate |
| gptkbp:bfsParent |
gptkb:Stuart–Prower_factor
|
| gptkbp:bfsLayer |
7
|
| http://www.w3.org/2000/01/rdf-schema#label |
Stuart–Prower syndrome
|