Search Results
Test Catalog
LNORO - Overview: Norovirus PCR, Molecular Detection, Feces
Diagnosing gastrointestinal disease (diarrhea or vomiting) caused by norovirus genogroups 1 and 2 This test should not be used as a test-of-cure.
NMHR1 - Overview: N-Methylhistamine, Random, Urine
Screening for and monitoring of mastocytosis and disorders of systemic mast-cell activation, such as anaphylaxis and other forms of severe systemic allergic reactions as a part of a random urine collection profile Monitoring therapeutic...
MSDW - Overview: Multiple Sulfatase Deficiency, Leukocytes
Supporting the biochemical diagnosis of multiple sulfatase deficiency in whole blood specimens This test is not useful for carrier detection.
RSBV - Overview: Rare Subepithelial Autoimmune Blistering Disease Variants, Serum
Aiding in the diagnosis of rare subepithelial autoimmune blistering diseases, including anti-laminin 332 pemphigoid, anti-p200 pemphigoid, epidermolysis bullosa acquisita, and systemic bullous lupus erythematosus
FFMSS - Overview: Maternal Serum Screening, Integrated, Specimen #1, PAPP-A, NT
Helpful to identify pregnancies at increased risk of having a child with Down Syndrome (DS), open neural tube defects (ONTD) and trisomy 18 (T18). This test is not diagnostic.
MOLD1 - Overview: Mold Panel, Serum
Establishing a diagnosis of an allergy to mold Defining the allergen responsible for eliciting signs and symptoms Identifying allergens: -Responsible for allergic response and/or anaphylactic episode -To confirm sensitization prior to...
PARVP - Overview: Parvovirus B19, Molecular Detection, PCR, Plasma
Diagnosing parvovirus B19 infection in plasma specimens
RPRT1 - Overview: Rapid Plasma Reagin (RPR) Screen with Reflex to Titer, Serum
Determining the current disease status Monitoring response to therapy for syphilis Aid to diagnose congenital syphilis This test cannot be used for testing spinal fluid specimens. This test is not intended for medical-legal use.
UPGD - Overview: Uroporphyrinogen Decarboxylase, Whole Blood
Preferred test for the confirmation of a diagnosis of porphyria cutanea tarda type II and hepatoerythropoietic porphyria
BILHA - Overview: Schistosoma species Antibody, IgG, Serum
Detection of antibodies to Schistosoma species
TXM - Overview: Toxoplasma gondii Antibody, IgM, Serum
Detecting recent infection with Toxoplasma gondii
TDP - Overview: Thiamine (Vitamin B1), Whole Blood
Assessment of thiamine deficiency Measuring thiamine levels in patients with behavioral changes, eye signs, gait disturbances, delirium, and encephalopathy; or in patients with questionable nutritional status, especially those who appear...
UPGC - Overview: Uroporphyrinogen III Synthase (Co-Synthase), Erythrocytes
Diagnosis of congenital erythropoietic porphyria This test is not useful for diagnosis of acute intermittent porphyria (AIP).
AN2TS - Overview: Antineuronal Nuclear Antibody Type 2 (ANNA-2) Titer, Serum
Investigating middle-aged or older patients who present with unexplainable signs of midbrain/cerebellar/brain stem disorder and/or myelopathy, especially women with a previous history of breast cancer, and both sexes if there is a history...
AN2TC - Overview: Antineuronal Nuclear Antibody Type 2 (ANNA-2) Titer, Spinal Fluid
Investigating middle-aged or older patients who present with unexplainable signs of midbrain/cerebellar/brain stem disorder and/or myelopathy, especially women with a previous history of breast cancer, and both sexes if there is a history...
AN1TC - Overview: Antineuronal Nuclear Antibody-Type 1 (ANNA-1) Titer, Spinal Fluid
Diagnosis of paraneoplastic autoimmune neuropathies, encephalomyeloradiculopathies, related neurologic disorders, and intestinal pseudo-obstruction/dysmotility associated with small-cell lung carcinoma Reporting an end titer result from...
23BPR - Overview: 2,3-Dinor 11 Beta-Prostaglandin F2 Alpha, Random, Urine
Screening for mast cell activation disorders including systemic mastocytosis using random urine specimens
WEED3 - Overview: Weed Panel # 3, Serum
Establishing a diagnosis of an allergy to English plantain, lamb's quarters, red sorrel, and Russian thistle allergen Defining the allergen responsible for eliciting signs and symptoms Identifying allergens: -Responsible for allergic...
WEED1 - Overview: Weed Panel # 1, Serum
Establishing a diagnosis of an allergy to English plantain, lamb's quarters, mugwort, Russian thistle, and short ragweed allergen Defining the allergen responsible for eliciting signs and symptoms Identifying allergens: -Responsible for...
Diagnosing syphilis
HERGM - Overview: HER2, Gastric/Esophageal, Semi-Quantitative Immunohistochemistry, Manual
Determining overexpression of HER2 protein of gastric and esophageal adenocarcinoma in formalin-fixed, paraffin-embedded tissue sections (with reflex to FISH testing)
FCDU2 - Overview: Benzodiazepines, Umbilical Cord Tissue
Benzodiazepines, Umbilical Cord Tissue
ZW347 - Overview: Miscellaneous Blueprint Genetics Inc.
Miscellaneous Blueprint Genetics Inc.
ZW346 - Overview: Miscellaneous Cleveland Clinic
Miscellaneous Cleveland Clinic
ZW321 - Overview: Miscellaneous Next Molecular Analytics
Miscellaneous Next Molecular Analytics
FDIRU - Overview: Diuretic Screen, Urine
Diuretic Screen, Urine
ZW1 - Overview: Miscellaneous MML Referral Test 1
Miscellaneous MML Referral Test 1
FIXCF - Overview: Immunofixation, CSF
Immunofixation, CSF
ZW143 - Overview: Miscellaneous IMMCO Diagnostics
Miscellaneous IMMCO Diagnostics
ZW299 - Overview: Miscellaneous Childrens Hospital Los Angeles
Miscellaneous Childrens Hospital Los Angeles
ZW298 - Overview: Miscellaneous IntrinsicDx
Miscellaneous IntrinsicDx
ZW305 - Overview: Misc Washington University Neuromuscular Clinical Lab
Misc Washington University Neuromuscular Clinical Lab
FSFM - Overview: Soluble Fibrin Monomer
Soluble Fibrin Monomer
GNBLC - Overview: Bleeding Disorders, Comprehensive Gene Panel, Next-Generation Sequencing, Varies
Evaluating hereditary bleeding in patients with a personal or family history suggestive of a hereditary bleeding disorder Confirming a hereditary bleeding disorder diagnosis with the identification of a known or suspected disease-causing...
CKDGP - Overview: Cystic Kidney Disease Gene Panel, Varies
Providing a genetic evaluation for patients with a personal or family history of cystic kidney disease Establishing a diagnosis of hereditary cystic kidney disease
Evaluation of known or suspected hematologic neoplasms, specifically of myeloid origin (eg, acute myeloid leukemia, myelodysplastic syndrome, myeloproliferative neoplasm, myelodysplastic/myeloproliferative neoplasm, unexplained cytopenias)...
CCMGG - Overview: Comprehensive Cardiomyopathy Gene Panel, Varies
Providing a genetic evaluation for patients with a personal or family history suggestive of a hereditary form of cardiomyopathy Establishing a diagnosis of a hereditary form of cardiomyopathy
ASOU - Overview: Arsenic Occupational Exposure, Random, Urine
Screening test for detection of occupational exposure to arsenic in random urine specimens
ASMW - Overview: Acid Sphingomyelinase, Leukocytes
Investigation of possible diagnosis of Niemann-Pick disease types A and B This test is not recommended for carrier detection because of the wide range of enzymatic activities observed in carriers and noncarriers.
ASCU - Overview: Arsenic/Creatinine Ratio, Urine
Screening for arsenic exposure using random urine specimens
LADV - Overview: Adenovirus, Molecular Detection, PCR, Varies
Aiding in the diagnosis of adenovirus infections
Identification of individuals who may be at risk for aminoglycoside-induced hearing loss (AIHL) Establishing a diagnosis of late-onset sensorineural hearing loss associated with aminoglycoside exposure Identifying mitochondrial variants...
ANA2 - Overview: Antinuclear Antibodies (ANA), Serum
Evaluating patients at-risk for antinuclear antibodies-associated systemic autoimmune rheumatic disease particularly systemic lupus erythematosus, Sjogren syndrome, and mixed connective tissue disease
AH50 - Overview: Alternative Complement Pathway, Functional, Serum
Investigation of suspected alternative pathway complement deficiency, atypical hemolytic uremic syndrome, C3 glomerulonephritis, and dense-deposit disease
CRCOF - Overview: Chromium and Cobalt, Synovial Fluid
Monitoring metallic prosthetic implant wear and local tissue destruction in failed hip arthroplasty constructs This test is not useful for assessment of vitamin B12 activity.
5INHE - Overview: Factor V Inhibitor Evaluation, Plasma
Detection and quantitation of inhibitors against coagulation factor V This test is not useful for the detection of a lupus-like circulating anticoagulant inhibitor, a nonspecific circulating anticoagulant, or other inhibitors that are not...
2INHE - Overview: Factor II Inhibitor Evaluation, Plasma
Detection and quantitation of inhibitor to factor II This test is not useful for the detection of a lupus-like circulating anticoagulant inhibitor, a nonspecific circulating anticoagulant, or other inhibitors that are not specific for...
10INE - Overview: Factor X Inhibitor Evaluation, Plasma
Detection and quantitation of inhibitor to coagulation factor X This test is not useful for the detection of a lupus-like circulating anticoagulant inhibitor, a nonspecific circulating anticoagulant, or other inhibitors that are not...
ENTP - Overview: Enterovirus, Molecular Detection, PCR, Plasma
Aiding in diagnosing enterovirus infections using plasma specimens This test should not be used to screen asymptomatic patients.
Aids in monitoring a previously confirmed diagnosis of B-cell acute lymphoblastic leukemia
Site Search
MCL - Trace Metals Analysis Specimen Collection and Transport - MC1235-233
MC1235-233rev0720Page 1 of 4©2020 Mayo Foundation for Medical Education and Research Trace Metals Analysis Specimen Collection and Transport Introduction Trace metals exist in our environment at concentrations...
lysosomal_storage_disorders_diagnostic_algorithm__part_1.pdf
Order: FUCW / Alpha-Fucosidase, Leukocytes Order 1 of the following: MPS4W / Mucopolysaccharidosis IV Enzyme Panel, Leukocytes ......
lysosomal-disorders-diagnostic-algorithm-part1.pdf
Order: FUCW / Alpha-Fucosidase, Leukocytes Order 1 of the following: ■ MPS4W / Mucopolysaccharidosis IV Enzyme Panel, Leukoc......
T800 MC4091-67CH MC4091-67CH.indd 1-2 11/14/2017 9:23:30 AM MC4091-67CH.indd 3-4 11/14/2017 9:23:30 AM...
inherited_motor_neuron_disease_testing_algorithm.pdf
Research (MFMER). All rights reserved. 12/2022 Spinal muscular atrophy (SMA) phenotype -SMA types 1-4 Order SMNDX / Spinal Muscular Atrophy Diagnostic Assay by Deletion/ Duplication Analysis Spinal bulbar...