Stuart-Prower factor deficiency
GPTKB entity
Statements (26)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
rare disease
coagulation disorder |
| gptkbp:affects |
blood clotting
|
| gptkbp:alsoKnownAs |
gptkb:Factor_X_deficiency
|
| gptkbp:causedBy |
mutation in F10 gene
|
| gptkbp:diagnosedBy |
prolonged activated partial thromboplastin time
factor X assay prolonged prothrombin time |
| gptkbp:firstDescribed |
1957
|
| https://www.w3.org/2000/01/rdf-schema#label |
Stuart-Prower factor deficiency
|
| gptkbp:ICD-10_code |
D68.1
|
| gptkbp:inheritance |
autosomal recessive
|
| gptkbp:namedAfter |
gptkb:Barbara_Prower
Edmond Stuart |
| gptkbp:OMIM |
227600
|
| gptkbp:prevalence |
very 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:Factor_X_deficiency
|
| gptkbp:bfsLayer |
7
|