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Factor X Deficiency
Factor x deficiency
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Related in the Kosmos
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Coagulation system
(34)
Activated protein C
Antithrombin
Coagulation factor
Factor II deficiency
Factor ix
Factor ix
Factor v deficiency
Factor vii deficiency
Factor viii
Factor xia
Factor xii deficiency
Factor xiii deficiency
Fibrinogen
Haemostasis
Protein Z
Prothrombin complex
Prothrombinase
Tenase
Thrombomodulin
Tissue factor
Tissue factor pathway inhibitor
Von willebrand factor
Bone hemostasis
Clot retraction
Cofact
Des-gamma carboxyprothrombin
Fibrinogenolysis
High-molec- ular-weight kininogen
Human Activated Protein C
Medical Laboratory Scientist
Platelet
Platelet activation
Prekallikrein
Protein S
Protein Z-related protease inhibitor
more...
EC 3.4.21
(28)
Kallikrein
Plasmin
Acrosin
Activated protein C
C3-convertase
C3-convertase
Chymotrypsin
Elastase
Enteropeptidase
Factor II deficiency
Factor ix
Factor vii deficiency
Factor xia
Factor xii deficiency
Fibrinolysin
Membrane-bound transcription factor peptidase, site 1
Pancreatic elastase
Prolyl endopeptidase
Prostate-specific antigen
Proteinase 3
Proteinase K
Reelin
Repressor lexA
Serine protease
Tissue plasminogen activator
Trypsin
Trypsin inhibitor
Tryptase
Urokinase
more...
Diseases and disorders
(44)
Fibromuscular dysplasia
Fast breathing
Hemophilia b
Floppy mitral valve
Fasciitis, necrotizing
Fasciitis, necrotizing
Familial spastic paraparesis
Hemophilia a
Fibrodysplasia ossificans progressiva
Familial dysbetalip- oproteinemia
Fibromyoma
Fish tapeworm
Fibrocystic breast disease
Fifth disease
Fragile x syndrome
Factor xi deficiency
Hemophilia
Folliculitis
Factor ix deficiency
Von willebrand disease
Prothrombin deficiency
Factor V Leiden
Fatty liver
Familial paroxysmal polyserositis
Female infertility
Familial dysautonomia
Thrombosis
Fetal alcohol syndrome
Parahemophilia
Microphthalmia
Frambesia tropica
Properdin deficiency
Fibrinogen deficiency
Protein c deficiency
Iodine deficiency
Hypoprocon- vertinemia
Activated protein c resistance
Fabry disease
Female pseudo-Turner syndrome
Glycogen storage disease
Fanconi anemia
Factor v deficiency
Factor vii deficiency
Factor xii deficiency
Antithrombin
more...
Genetic disorders
(13)
Fibromuscular dysplasia
Familial spastic paraparesis
Hemophilia a
Fragile x syndrome
Factor xi deficiency
Factor xi deficiency
Hemophilia
Von willebrand disease
Familial paroxysmal polyserositis
Microphthalmia
Activated protein c resistance
Fabry disease
Female pseudo-Turner syndrome
Fanconi anemia
more...
Blood disorders
Hemophilia b
Hemophilia a
Factor xi deficiency
Hemophilia
Von willebrand disease
Genes associated with genetic disorders
(14)
ASPM (Gene)
Common gamma chain
Cystic fibrosis transmembrane conductance regulator
DAB1
Factor ix
Factor ix
Factor viii
Factor xia
Huntingtin
Ifi202
Parkin (ligase)
Phenylalanine hydroxylase
Research of Down syndrome-related genes
Usher 1C
ΔF508
more...
Hematology
(12)
Cryoprecipitate
Bleeding disorders
Thrombophilia
Lupus anticoagulant
Fondaparinux
Fondaparinux
Activated protein C
Factor V Leiden
Haemostasis
Thrombosis
Von willebrand factor
Protein c deficiency
Activated protein c resistance
more...
Blood products
(13)
Fresh frozen plasma
Blood banks
Blood plasma
Bloodmobile
Cofact
Cofact
Cryoprecipitate
Hepatitis B immune globulin
Placenta cord banking
Plasmapheresis
Platelet
Platelet-rich plasma
Prothrombin complex
Whole blood
more...
Fibrinolytic system
(12)
Fibrinolysis
Plasminogen activator inhibitor 1
Alpha 2-antiplasmin
Anistreplase
Antifibrinolytics
Antifibrinolytics
D-dimer
Hyperfibrinolysis
Plasmin
Plasminogen activator inhibitor-2
Reteplase
Thrombin-a- ctivatable fibrinolysis inhibitor
Tissue plasminogen activator
more...
Symptoms
(8)
Bleeding into joints
Prolonged bleeding
Mucous membrane bleeding
Mucous membrane
Muscle
Muscle
Muscle bleeding
Severe bleeding
Fast breathing
more...
Coagulation
(25)
Procoagulant
Intrinsic pathway
KLK1
KLK10
KLK11
KLK11
KLK12
KLK13
KLK14
KLK15
KLK2
KLK4
KLK5
KLK6
KLK7
KLK8
KLK9
Plasminogen activator
Thrombin
Factor XII
Factor XI
Kallikrein
Plasmin
Prostate-specific antigen
Tissue plasminogen activator
Urokinase
more...
See also
(20)
Familial hypertrigl- yceridemia
Friedreich
Fibrosing alveolitis
Fenestrations
Vitamin k deficiency
Vitamin k deficiency
People with hemophilia
Familial
APTT
X-linked recessive
X linked
Novoseven
Fluoridation
Fish oils
Corneal dystrophy
Fluorhydric acid
GLA domain
Floaters
Vibration white finger
Acute
Amyloidosis
more...
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