Disease Comparison Results (show all mode) for Factor V Leiden mutation and Protein-C deficiency

Ads

Protein-C deficiency

Found: 59 | Differences: 27

Factor V Leiden mutation

Found: 49 | Differences: 17

Factor V Leiden mutation and Protein-C deficiency sharing 32 common findings. (show all, show common, show differences)

Clinical Manifestations
Signs & Symptoms
Signs of phlebitis in leg
Stroke Syndrome Child
Clinical Presentation & Variations
Presentation/Warfarin Insensitivity Tolerance
Presentation/Deep Vein Thrombosis Young Recurrent
Presentation/Thrombophlebitis Hereditary Recurrent
Presentation/Pulmonary Embolism Recurrent
Disease Progression
Course/Chronic disorder
Course/Chronic only
Demographics & Risk Factors
Established Disease Population
Patient/Protein C deficiency
Population Group
Child
Population/Pediatrics population
Family History
Family history/Thrombosis/DVT/Deaths
Sex & Age Groups
Population/Child
Population/Children/all
Laboratory Tests
Abnormal Lab Findings - Decreased
Protein C level/blood (Lab)
Abnormal Lab Findings - Increased
Fibrin Degredation Product (FDP) (Lab)
Fibrin Split Products/FSP/Dimers/Monomers (Lab)
FibrinPeptide A
Soluble Fibrin Monomers [LAB]
Associated Diseases & Rule outs
Associated Disease & Complications - Rule Outs
Antiphospholipid Syndrome/APLS
Associated Disease & Complications - Causes
Cerebral vascular accident
Cerebral vein thrombosis/phlebitis
Hepatic vein thrombosis (Budd-Chiari)
Hypercoagulability/Thrombophilia
Mesenteric vein thrombosis
Protein C deficiency
Pulmonary embolism
Purpura fulminans
Retinal vein thrombosis, central
Stroke Syndromes/Atypical causes
Stroke/Child
Thromboembolic disease
Thrombophlebitis Arm/Deep Vein
Thrombophlebitis, deep vein
Transient ischemic attack/cerebral
Warfarin induced/skin necrosis
Hypercoaguability
Disease Mechanism & Classification
Class
CLASS/Hematologic (category)
Pathophysiology
Pathophysiology/Gene locus 2q13-q14
Pathophysiology/Gene locus Chromosome 2
Pathophysiology/Gene Locus Identified/OMIM database
Pathophysiology/Genomic indentifiers (polymorphism/snip/mutations)
Pathophysiology/Hereditary disease/Adult manifestations
Pathophysiology/Thrombosis veins lower ext/iliac/femoral
Pathophysiology/Antithrombin III defect/deficiency
Pathophysiology/Intravasular coagulation process
Pathophysiology/Spontaneous Coagulation
Pathophysiology/Ischemic optic neuritis
Process
PROCESS/Autosomal dominant hereditary disease (ex).
PROCESS/Enzyme defect/Metabolic disorder (ex)
PROCESS/Hereditofamilial (category)
PROCESS/Metabolic/storage disorder (category)
PROCESS/Coagulation derangement/disorder (ex)
PROCESS/Hereditary hypercoagulation/thrombosis disorders (ex)
Treatment
Drug Therapy - Contraindication
RX/Oral contraceptive
Drug Therapy - Indication
RX/Anticoagulants
RX/Coumarin/derivatives
RX/Warfarin (Coumadin)
Clinical Manifestations
Signs & Symptoms
Moro Reflex unilateral Abnormal
Stroke Syndrome Child
Clinical Presentation & Variations
Presentation/Deep Vein Thrombosis Young Recurrent
Presentation/Thrombophlebitis Hereditary Recurrent
Presentation/Pulmonary Embolism Recurrent
Disease Progression
Course/Chronic disorder
Course/Chronic only
Demographics & Risk Factors
Ethnic or Racial Factors
European racial stock/population
Population Caucasian/White
Population Group
Child
Population/Pediatrics population
Family History
Family history/Thrombosis/DVT/Deaths
Sex & Age Groups
Population/Child
Population/Children/all
Laboratory Tests
Abnormal Lab Findings (Non Measured)
Activated Protein C inhibition finding (Lab)
Chromosomal abnormality (Lab)
DNATest specific/genetics laboratory/abnormality (Lab)
Abnormal Lab Findings
PTT/Partial Thromboplastin Time/Activated PTT (Lab)
Associated Diseases & Rule outs
Associated Disease & Complications - Rule Outs
Antiphospholipid Syndrome/APLS
Associated Disease & Complications - Causes
Cerebral vein thrombosis/phlebitis
Factor V Leiden mutation disease
Hepatic vein thrombosis (Budd-Chiari)
Hypercoagulability/Thrombophilia
Mesenteric vein thrombosis
Preeclampsia of pregnancy
Pulmonary embolism
Pulmonary embolism, recurrent/Homans disease
Stroke/Child
Thromboembolic disease
Thrombophlebitis Arm/Deep Vein
Thrombophlebitis, deep vein
Hypercoaguability
Disease Mechanism & Classification
Class
CLASS/Hematologic (category)
Pathophysiology
Pathophysiology/Genomic indentifiers (polymorphism/snip/mutations)
Pathophysiology/Hereditary disease/Adult manifestations
Pathophysiology/Activated protein C resistant factor V
Pathophysiology/Factor V APC resistance
Pathophysiology/Factor V:Q506-GLN sequence DNA abnormal
Pathophysiology/Intravasular coagulation process
Pathophysiology/Spontaneous Coagulation
Process
PROCESS/Clots/thrombi disorder (ex)
PROCESS/Hereditofamilial (category)
PROCESS/Thrombophlebitis process (ex)
PROCESS/Coagulation derangement/disorder (ex)
PROCESS/Hereditary hypercoagulation/thrombosis disorders (ex)
Treatment
Drug Therapy - Contraindication
RX/Oral contraceptive
Other Treatments
TX/Lifetime anticoagulation
Ads