|
gptkbp:instanceOf
|
rare bleeding disorder
|
|
gptkbp:acquiredCausedBy
|
gptkb:liver_disease
gptkb:vitamin_K_deficiency
amyloidosis
|
|
gptkbp:affects
|
blood coagulation
|
|
gptkbp:alsoKnownAs
|
gptkb:Stuart-Prower_factor_deficiency
|
|
gptkbp:canBe
|
congenital
acquired
|
|
gptkbp:causedBy
|
mutation in F10 gene
|
|
gptkbp:complication
|
intracranial hemorrhage
joint bleeding
|
|
gptkbp:diagnosedBy
|
prolonged activated partial thromboplastin time
factor X assay
prolonged prothrombin time
|
|
gptkbp:firstDescribed
|
1953
|
|
https://www.w3.org/2000/01/rdf-schema#label
|
Factor X deficiency
|
|
gptkbp:ICD-10_code
|
D68.1
|
|
gptkbp:inheritance
|
autosomal recessive
|
|
gptkbp:namedAfter
|
gptkb:Barbara_Prower
gptkb:Edmund_Stuart
|
|
gptkbp:OMIM
|
227600
|
|
gptkbp:prevalence
|
very rare
|
|
gptkbp:relatedTo
|
gptkb:hemophilia_B
gptkb:hemophilia_A
gptkb:factor_VII_deficiency
gptkb:factor_V_deficiency
|
|
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
|
|
gptkbp:bfsLayer
|
6
|