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

Clinical
Demographics
Lab
Diseases
Classification
Synonyms
Treatment
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Hemophagocytic lymphohistiocytosis (HLH)

Found: 23 | Differences: 21

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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