Disease Comparison Results (show all mode) for Factor II mutation (20210) and Thyrotoxic periodic paralysis

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Thyrotoxic periodic paralysis

Found: 42 | Differences: 42

Factor II mutation (20210)

Found: 36 | Differences: 36

Factor II mutation (20210) and Thyrotoxic periodic paralysis do not share any common findings.

Clinical Manifestations
Signs & Symptoms
Tachycardia/Fast heart rate
Muscle weakness
Symmetrical muscle/pain, weakness
Weak/Weak as a kitten (symptom)
Intermittant flaccid paralysis
Paralysis
Tremor
Tremor,fine
Tremulousness
Weakness/Diffuse motor loss
Enervated/extreme acute fatigue
Weakness
Weakness non-neuromuscular/systemic
Disease Progression
Course/Attack/Brief/Two hours usual
Course/Attacks Episodic Spells
Course/Attacks last 1 to 2 days
Course/Periodic Episodic
Demographics & Risk Factors
Ethnic or Racial Factors
Asian population
Chinese population
Past History
Past history/Thyrotoxicosis
Established Disease Population
Patient/Graves disease/thyrotoxicosis
Patient/Thyrotoxicosis
Population Group
Man
Population/Immigrant population
Sex & Age Groups
Population/Adult/all
Population/Male
Population/Man patient
Population/Thirties adult
Laboratory Tests
Abnormal Lab Findings - Decreased
Potassium, serum (Lab)
Abnormal Lab Findings - Increased
Thyroxin/T4 (Lab)
Tri-iodothyronine/T3 as Resin Uptake (Lab)
Associated Diseases & Rule outs
Associated Disease & Complications - Rule Outs
Hypokalemia
Hypokalemic periodic paralysis
Muscular dystrophy
Associated Disease & Complications - Causes
Periodic paralysis syndrome
Thyrotoxic periodic paralysis
Disease Synergy
Synergy/Carbohydrate excess/diet
Synergy/Cold environment
Synergy/Rest/after vigorous exercise
Synergy/Salt load/high sodium diet
Disease Mechanism & Classification
Process
PROCESS/Ethnic predilection (ex)
Synonyms
Synonym
Synonym/TPP/Thyrotoxic periodic paralysis
Clinical Manifestations
Signs & Symptoms
Moro Reflex unilateral Abnormal
Stroke Syndrome Child
Clinical Presentation & Variations
Presentation/Deep Vein Thrombosis Young Recurrent
Presentation/Thrombophlebitis Hereditary 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)
Chromosomal abnormality (Lab)
ProThrombin mutation factor II/20210 abnormality (Lab)
Associated Diseases & Rule outs
Associated Disease & Complications - Rule Outs
Antiphospholipid Syndrome/APLS
Associated Disease & Complications - Causes
Factor II mutation (20210) disease
Hepatic vein thrombosis (Budd-Chiari)
Hypercoagulability/Thrombophilia
Mesenteric vein thrombosis
Stroke/Child
Thromboembolic disease
Thrombophlebitis Arm/Deep Vein
Thrombophlebitis, deep vein
Disease Mechanism & Classification
Class
CLASS/Hematologic (category)
Pathophysiology
Pathophysiology/Genomic indentifiers (polymorphism/snip/mutations)
Pathophysiology/Intravasular coagulation process
Pathophysiology/Spontaneous Coagulation
Process
PROCESS/Autosomal recessive disorder (ex)
PROCESS/Hereditofamilial (category)
PROCESS/Coagulation derangement/disorder (ex)
Synonyms
Synonym
Synonym/FII-20210 mutation
Treatment
Drug Therapy - Contraindication
RX/Oral contraceptive
Drug Therapy - Indication
RX/Anticoagulants
RX/Warfarin (Coumadin)
Other Treatments
TX/Lifetime anticoagulation
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