factor X deficiency

GPTKB entity

Statements (23)
Predicate Object
gptkbp:instanceOf bleeding disorder
coagulation disorder
gptkbp:causedBy mutation in F10 gene
gptkbp:diagnosedBy prolonged activated partial thromboplastin time
prolonged prothrombin time
factor X activity assay
gptkbp:firstDescribed 1950s
https://www.w3.org/2000/01/rdf-schema#label factor X deficiency
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