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Showing search results for "algorithm" 31-40 of 313
- JAK2 Exons 12 and 13 Mutations, Qualitative, Leumeta
Myeloproliferative disorders (MPDs) are clonal hematopoietic stem cell malignancies characterized by excessive production of blood cells by hematopoietic precursors. In addition to thrombotic and hemorrhagic …... More
- Factor V (Leiden) Mutation Analysis
Factor V (Leiden) Mutation is a point mutation that causes resistance of Factor V protein degradation by activated protein C (APC). This mutation is associated with increased risk of venous thrombosis.... More
- Factor VIII Activity, Chromogenic
Preferred test in patients with Lupus anticoagulant, on heparin or direct thrombin inhibitors, or on Factor VIII concentrates.... More
- Factor VIII Activity, Clotting
This test is useful to evaluate a prolonged aPTT. The most common form of hemophilia is caused by a deficiency of Factor VIII. Hemophilia A is an X-linked disorder affecting between 1 in 5000 to 10000 males.... More
- Factor V HR2 Allele DNA Mutation Analysis
Factor V HR2 Allele, DNA Mutation Analysis is useful in patients who are carriers of Factor V Mutation (Leiden). Coinheritance of Factor V Mutation (Leiden) is associated with a 3-4-fold increased risk of venous …... More
- Cardiolipin Antibodies(IgG, IgM)
Cardiolipin antibodies (CA) are detected in a subgroup of patients with autoimmune disorders, particularly Systemic Lupus Erythematosus (SLE), who are at risk for vascular thrombosis, thrombocytopenia, cerebral infarct …... More
- Cardiolipin Antibody (IgA)
Cardiolipin antibodies (CA) are seen in a subgroup of patients with autoimmune disorders, particularly Systemic Lupus Erythematosus (SLE), who are at risk for vascular thrombosis, thrombocytopenia, cerebral infarct and/…... More
- 11-Deoxycortisol, LC/MS/MS
11-Deoxycortisol (Compound S) is useful in diagnosing patients with 11-beta-hydroxylase deficiency (second leading cause of congenital adrenal hyperplasia) and primary (adrenal failure) or secondary (hypothalamic-…... More
- Chronic Lymphocytic Leukemia (CLL)/Lymphoma Diagnostic Panel
To aid in the diagnosis, lineage assignment, subclassification, and response to treatment of hematologic malignancies.... More
- Canavan Disease Mutation Analysis
Canavan Disease is an autosomal recessive disease that results in demyelination and spongy degeneration of the brain. Canavan Disease carrier rate is approximately 1 in 40 among those of Ashkenazi Jewish heritage. This …... More
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