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- Disease Information
- Disease Comparison
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Disease Processes ▼
- Auto Immune
- Vascular-Arteriosclerosis
- Biochemical
- Congenital-developmental
- Deficiency
- Degenrative-Necrosis
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Major Organs-Systems ▼
- Systemic
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Disease Information for Factor X deficiency (Stuart-Power factor)
- Clinical Manifestations
- Signs & Symptoms
- Flooding menstrual bleeding
- Disease Progression
- Course/Chronic disorder
- Demographics & Risk Factors
- Population Group
- Child
- Population/Pediatrics population
- Family History
- Family history/Bleeding disorders
- Family history/Blood disease
- Sex & Age Groups
- Population/Child
- Population/Child-Infant Only
- Population/Children/all
- Laboratory Tests
- Abnormal Lab Findings (Non Measured)
- Clotting factor assay/abnormal (Lab)
- Coagulation/Clotting factors decreased (Lab)
- Abnormal Lab Findings - Decreased
- Factor 10 (Stuart Prower) (Lab)
- Abnormal Lab Findings - Increased
- Clotting time/Activated clotting time test (Lab)
- PIVKA II/Acarboxyprothrombin level (Lab)
- Prothrombin consumption (Lab)
- PT -Prothrombin time (Lab)
- Thromboplastin generation time (Lab)
- Associated Diseases & Rule outs
- Associated Disease & Complications
- Bleeding complications/Surgery
- Muscle Hematoma
- Postpartum hemorrhage
- Disease Mechanism & Classification
- Class
- CLASS/Hematologic (category)
- Pathophysiology
- Pathophysiology/Genomic indentifiers (polymorphism/snip/mutations)
- Process
- PROCESS/Hereditofamilial (category)
- PROCESS/Coagulation derangement/disorder (ex)
- Synonyms
- Synonym
- DEFIC FACTOR X, DEFIC STUART PROWER, DEFIC STUART PROWER FACTOR, Deficiencies Factor X, Deficiency factor X, Deficiency Stuart Prower, Deficiency Stuart Prower Factor, Disease Stuart Prower, FACTOR X DEFIC, Factor X Deficiencies, Factor X Deficiency, Factor X deficiency (disorder), Stuart, STUART PROWER DEFIC, Stuart Prower Deficiency, STUART PROWER FACTOR DEFIC, Stuart Prower factor deficienc, Stuart Prower Factor Deficiency, Synonym/Stuart-Prower factor deficiency
- Definition
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Blood coagulation disorder usually inherited as an autosomal recessive trait, though it can be acquired. It is characterized by defective activity in both the intrinsic and extrinsic pathways, impaired thromboplastin time, and impaired prothrombin consumption.
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- External Links Related to Factor X deficiency (Stuart-Power factor)
- Wikipedia
- Merck
- Images
- PubMed (National Library of Medicine)
- NGC (National Guideline Clearinghouse)
- Medscape (eMedicine)
- Harrison's Online (accessmedicine)
- NEJM (The New England Journal of Medicine)