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Showing search results for "algorithm" 81-90 of 312

  1. Centromere B Antibody

    Centromere B Antibody is diagnostic for the form of scleroderma known as CREST (calcinosis, Raynaud's phenomenon, esophageal immotility, sclerodactyly, and telangiectasia).... More

  2. Cardio IQ ASCVD Risk Panel with Score

    This panel provides the 10-year and lifetime risk of atherosclerotic cardiovascular disease (ASCVD) using lipid results with anthropomorphic data and family history. The ASCVD risk assessment is recommended in the 2013…... More

  3. CAH (21-Hydroxylase Deficiency) Gene Sequencing

    This DNA sequencing test identifies rare variants in the 21-hydroxylase gene known to cause congenital adrenal hyperplasia (CAH). It is used when individuals are known or suspected to have 21-OH pathogenic variants …... More

  4. Cystic Fibrosis Complete Rare Variant Analysis, Entire Gene Sequence

    Cystic fibrosis (CF) is the most common recessive lethal genetic disorder affecting primarily Caucasians of Northern European descent, with an incidence of approximately 1 in 3300 births and a carrier rate of 1 in 29. …... More

  5. CEA

    Increased serum CEA levels have been detected in persons with primary colorectal cancer and in patients with other malignancies involving the gastrointestinal tract, breast, lung, ovarian, prostatic, liver and …... More

  6. Chromosome Analysis, Hematologic Malignancy

    Cytogenetics of hematologic disorders attempts to define and interpret chromosomal aberrations that occur in neoplastic cells associated with leukemia, lymphoma and other hematologic malignancies. Chromosome …... More

  7. Calcitonin

    Calcitonin concentration is increased in patients with medullary thyroid carcinoma. Calcitonin concentrations may be used to monitor disease.... More

  8. CAH (21-Hydroxylase Deficiency) Common Mutations

    This test identifies mutations in the 21-hydroxylase gene known to cause congenital adrenal hyperplasia (CAH). It is used to: 1) confirm or establish a diagnosis of CAH due to 21-OH deficiency; 2) identify genetic …... More

  9. c-KIT Mutation Analysis, Cell Based

    Activating c-KIT mutations have been indentified in various human cancers. c-KIT exon 8 and 17 mutations have been described in patients with CBF-AMLs and usually confer a poor prognosis with increased relapse rate. c-…... More

  10. Childhood Allergy (Food and Environmental) Profile: Puerto Rico

    Childhood Allergy (Food and Environmental) Profile: Puerto Rico CPT Code(s) 82785, 86003 (x12) Includes IgE allergy testing for: Alternaria alternata (m6) Cat Dander (e1) Cockroach (i6) Corn (f8) Cow's Milk (f2) …... More

* The tests listed by specialist are a select group of tests offered. For a complete list of Quest Diagnostics tests, please refer to our Directory of Services.