NSAI - Overview: Neurosyphilis IgG, Antibody Index, Spinal Fluid
Aid in the diagnosis of neuroinvasive syphilis as part of a profile
RRPRS - Overview: Rapid Plasma Reagin Screen with Reflex to Titer, Serum
Aid for the diagnosis of infection with Treponema pallidum Rapid plasma reagin testing following a positive treponemal antibody test This test is not useful as a screening or confirmatory test for blood donor specimens.
FPOLO - Overview: Poliovirus (Types 1, 3) Antibodies, Neutralization
Poliovirus (Types 1, 3) Antibodies, Neutralization
FWARP - Overview: Warfarin, Plasma
Warfarin, Plasma
FHC18 - Overview: 18-Hydroxycorticosterone, Serum
18-Hydroxycorticosterone, Serum
Corn IgG4
Pork IgG4
FGHSU - Overview: Gamma-Hydroxybutyric Acid (GHB), Urine
Gamma-Hydroxybutyric Acid (GHB), Urine
FGANP - Overview: Ganciclovir, Plasma
Ganciclovir, Plasma
FEWG4 - Overview: Egg White IgG4
Egg White IgG4
FGFP2 - Overview: IgG4 Food Panel II
IgG4 Food Panel II
FACEC - Overview: Angiotensin Converting Enzyme, CSF
Support diagnosis of neurosarcoidosis. May be used to evaluate treatment response.
FASPG - Overview: Aspergillus IgG Precipitins Panel
Aspergillus IgG Precipitins Panel
FMVCO - Overview: MVista Coccidioides Quantitative Antigen EIA
MVista Coccidioides Quantitative Antigen EIA
FNAD - Overview: Nadolol, Serum/Plasma
Nadolol, Serum/Plasma
FHCCF - Overview: THC Confirmation, MS, SP
THC Confirmation, MS, SP
FMETN - Overview: Metformin, Plasma
Metformin, Plasma
FBFPI - Overview: Bird Fancier's Precipitin Panel I
Bird Fancier's Precipitin Panel I
FCATB - Overview: Carotene, Beta
Confirming the diagnosis of carotenoderma Detecting fat malabsorption Depressed carotene levels may be found in cases of steatorrhea.
FLDLD - Overview: LDL Cholesterol, Direct
LDL Cholesterol, Direct
FC4AL - Overview: C4 Level by RIA
C4 Level by RIA
FC3AR - Overview: C3a Level By RIA
C3a Level By RIA
GNVWD - Overview: von Willebrand Disease, VWF and GP1BA Genes, Next-Generation Sequencing, Varies
Evaluating von Willebrand disease and platelet-type von Willebrand disease in patients with a personal or family history suggestive of von Willebrand disease Confirming von Willebrand disease or platelet-type von Willebrand disease...
GNHTC - Overview: Hereditary Thrombocytopenia Gene Panel, Next-Generation Sequencing, Varies
Evaluating hereditary thrombocytopenia disorders in patients with a personal or family history suggestive of a hereditary thrombocytopenia disorder Diagnosing hereditary thrombocytopenia disorders for patients in whom phenotypic testing is...
PCGP - Overview: Porphyria Comprehensive Gene Panel, Varies
Follow up for abnormal biochemical results suggestive of porphyria Establishing a molecular diagnosis for patients with porphyria Identifying variants within genes known to be associated with porphyria, allowing for predictive testing of...
GNF11 - Overview: Hemophilia C (Factor XI Deficiency), F11 Gene, Next-Generation Sequencing, Varies
Evaluating factor XI deficiency (FXID) in patients with a personal or family history suggestive of FXID Confirming an FXID diagnosis with the identification of known or suspected disease-causing alterations in the F11 gene Determining...
ENDCP - Overview: Hereditary Endocrine Cancer Panel, Varies
Evaluating patients with a personal or family history suggestive of a hereditary endocrine tumor syndrome Establishing a diagnosis of a hereditary endocrine tumor syndrome, allowing for targeted surveillance based on associated risks...
Screening for infection with high-risk human papillomavirus (HPV) associated with the development of cervical cancer Individual genotyping of HPV-16 and/or HPV-18 if present This testing is intended for use in clinical monitoring and...
GNF13 - Overview: Factor XIII Deficiency, F13A1 and F13B Genes, Next-Generation Sequencing, Varies
Evaluating factor XIII deficiency (FXIIID) in patients with a personal or family history suggestive of FXIIID Confirming an FXIIID diagnosis with the identification of known or suspected disease-causing alterations in the F13A1 or F13B...
CDGGP - Overview: Congenital Disorders of Glycosylation Gene Panel, Varies
Establishing a molecular diagnosis for patients with congenital disorders of glycosylation Identifying variants within genes known to be associated with congenital disorders of glycosylation, allowing for predictive testing of at-risk...
CHLGP - Overview: Cholestasis Gene Panel, Varies
Establishing a molecular diagnosis for patients with monogenic cholestasis Identifying variants within genes known to be associated with primary, monogenic cholestasis, allowing for predictive testing of at-risk family members This panel...
SSH24 - Overview: Supersaturation Profile, Self-Collect, 24 Hour, Urine
Diagnosis and management of patients with renal lithiasis: -Predicting the likely composition of the stone, in patients who have a radiopaque stone, for whom stone analysis is not available -May aid in designing a treatment program Aiding...
REVE2 - Overview: Erythrocytosis Evaluation, Blood
Definitive, comprehensive, and economic evaluation of an individual with JAK2-negative erythrocytosis associated with lifelong sustained increased hemoglobin or hematocrit
HBEL1 - Overview: Hemoglobin Electrophoresis Evaluation, Blood
Diagnosis and classification of hemoglobin disorders, including thalassemias and hemoglobin variants
PINP - Overview: Procollagen I Intact N-Terminal, Serum
Aiding in monitoring antiresorptive and anabolic therapy in patients with osteoporosis An adjunct in the assessment of conditions associated with increased bone turnover, such as Paget disease This test should not be used as a screening...
PNP - Overview: Platelet Neutralization Procedure, Plasma
Aiding in the confirmation or exclusion of the presence of a lupus anticoagulant (LAC) inhibitor when used in conjunction with other appropriate coagulation tests. Aids in differentiating deficiencies or inhibitors of specific coagulation...
OCT2 - Overview: OCT-2 Immunostain, Technical Component Only
Classification of lymphomas
PHTDP - Overview: Phosphorylated TDP43 Immunostain, Technical Component Only
Identification of pathological forms of TDP-43 in neurodegenerative diseases
PK1 - Overview: Pyruvate Kinase Enzyme Activity, Blood
Evaluation of nonspherocytic hemolytic anemia Evaluation of neonatal anemia or jaundice Evaluation of unexplained noninfectious hepatic failure Evaluation of unexplained iron overload Evaluation of unusually severe hemoglobin S...
PTNT - Overview: Prothrombin G20210A Mutation, Blood
Patients with clinically suspected thrombophilia Determination of the duration of anticoagulation therapy of venous thromboembolism patients Screening for women contemplating hormone therapy
PTEN - Overview: Phosphatase and Tensin Homolog (PTEN) Immunostain, Technical Component Only
Diagnosis of intraductal prostate carcinoma
TGII - Overview: Thyroglobulin, Interference Interpretation
Interpretation for the evaluation of suspected interference from heterophile antibodies causing a falsely elevated thyroglobulin result
TRAP - Overview: Tartrate-Resistant Acid Phosphatase (TRAP) Immunostain, Technical Component Only
Classification of leukemias and lymphomas
WNGC - Overview: West Nile Virus Antibody, IgG, Spinal Fluid
Aids in diagnosing recent or past central nervous system West Nile virus infection
VEGF - Overview: Vascular Endothelial Growth Factor, Plasma
Evaluation of patients with suspected POEMS (polyneuropathy, organomegaly, endocrinopathy, monoclonal gammopathy, and skin changes) syndrome, particularly in differentiating from other forms of polyneuropathy and/or monoclonal plasma cell...
Diagnosing fat malabsorption due to pancreatic or intestinal disorders Monitoring effectiveness of enzyme supplementation in certain malabsorption disorders This test is not useful for differentiating among pancreatic diseases.
VITK1 - Overview: Vitamin K1, Serum
Assessment of circulating vitamin K1 concentration.
RALB1 - Overview: Albumin, Random, Urine
Assessing the potential for early onset of nephropathy in diabetic patients using random urine specimens
AMMO - Overview: Ammonium, 24 Hour, Urine
Diagnosis of the cause of acidosis Diagnosis and treatment of kidney stones
ORTHP - Overview: Orthostatic Proteinuria, Random, Urine
Diagnosis of orthostatic proteinuria
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