Disease Comparison Results (show all mode) for Factor V Leiden mutation and Hemophagocytic lymphohistiocytosis (HLH)

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Hemophagocytic lymphohistiocytosis (HLH)

Found: 23 | Differences: 21

Factor V Leiden mutation

Found: 49 | Differences: 47

Factor V Leiden mutation and Hemophagocytic lymphohistiocytosis (HLH) sharing 2 common findings. (show all, show common, show differences)

Clinical Manifestations
Signs & Symptoms
Lymphadenopathy Systemic
Associated Diseases & Rule outs
Associated Disease & Complications
EBV/B-cell Lymphoproliferative syndrome
Disease Mechanism & Classification
Class
CLASS/Immune System Disorder (ex)
Pathophysiology
Pathophysiology/Gene locus 10q21-q22
Pathophysiology/Gene locus 10q22
Pathophysiology/Gene locus 9q21.3-q22
Pathophysiology/Gene locus Chromosome 10
Pathophysiology/Gene locus Chromosome 9
Pathophysiology/Gene Locus Identified/OMIM database
Pathophysiology/Genomic indentifiers (polymorphism/snip/mutations)
Pathophysiology/Histiocyte/macrophage disorder (ex)
Pathophysiology/Specific immune defect for EBV
Process
PROCESS/Hereditary Multiple anomalies syndrome [EX]
PROCESS/Hereditofamilial (category)
PROCESS/Hypertrophic/Hyperplastic disorder (ex)
PROCESS/INCIDENCE/Extremely rare disease
PROCESS/Immune system disorder (ex)
Synonyms
Synonym
Synonym/FEL
Synonym/Hemophagocytic lymphohistiocytosis, familial
Synonym/HLH
Synonym/Lymphadenitis/hemophagocytic histiocytosis
Synonym/Massive Lymphadenopathy Syndrome
Synonym/Sinus Histiocytosis
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
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