FPAB - Overview: Vitamin B5 (Pantothenic Acid) Bioassay

Vitamin B5 (Pantothenic Acid) Bioassay

FCBDS - Overview: Cannabidiol, Serum

Cannabidiol, Serum

FRFIT - Overview: Rabies Antibody Endpoint

Rabies Antibody Endpoint

PMSBB - Overview: Postmortem Screening, Bile and Blood Spot

Postmortem evaluation of individuals at any age who died suddenly or unexpectedly; testing is particularly recommended under the following circumstances (risk factors): -Family history of sudden infant death syndrome or other sudden...

GUSBB - Overview: Beta-Glucuronidase, Blood Spot

Supporting the biochemical diagnosis of mucopolysaccharidosis VII (MPS VII, Sly syndrome) This test is not useful for determining carrier status for MPS VII.

ALAD - Overview: Aminolevulinic Acid Dehydratase, Whole Blood

Preferred confirmation test for the diagnosis of aminolevulinic acid dehydratase deficiency porphyria This test is not useful for detecting lead intoxication.

ALKP - Overview: Alkaline Phosphatase, Total and Isoenzymes, Serum

Aid in the diagnosis and treatment of liver, bone, intestinal, and parathyroid diseases Determining the tissue source of increased alkaline phosphatase (ALP) activity in serum Differentiating between liver and bone sources of elevated ALP

ARSBW - Overview: Arylsulfatase B, Leukocytes

Supporting the biochemical diagnosis of mucopolysaccharidosis type VI (MPS VI, Maroteaux-Lamy syndrome) in whole blood specimens This test is not useful for carrier detection.

I2SWB - Overview: Iduronate-2-Sulfatase, Leukocytes

Supporting the biochemical diagnosis of mucopolysaccharidosis II (MPS II; Hunter syndrome) in whole blood specimens This test is not useful for carrier detection for MPS II.

JCPCR - Overview: JC Virus, Molecular Detection, PCR, Spinal Fluid

Aiding in diagnosing progressive multifocal leukoencephalopathy due to JC virus This test is not to be used as a diagnostic tool for Creutzfeldt-Jakob disease This test is not recommended for screening asymptomatic patients

JO1 - Overview: Jo 1 Antibodies, IgG, Serum

Evaluating patients with clinical features of idiopathic inflammatory myositis, especially those with clinical features suggestive of anti-synthetase syndrome or interstitial lung disease

BRAFB - Overview: Cell-Free DNA BRAF V600, Blood

An alternative to invasive tissue biopsies for the determination of BRAF V600E and V600K alterations Identification of patients with cancer who are most likely to benefit from targeted therapies This test is not intended for serial...

OAUS - Overview: Organic Acids Screen, Urine Spot

Diagnosis of inborn errors of metabolism using dried urine specimens

NCLW - Overview: Neuronal Ceroid Lipofuscinosis, Two-Enzyme Panel, Leukocytes

Supporting the biochemical diagnosis of two neuronal ceroid lipofuscinoses, CLN1 and CLN2 in whole blood specimens This test is not useful for carrier detection.

OAU - Overview: Organic Acids Screen, Random, Urine

Diagnosis of inborn errors of metabolism

PPFE - Overview: Protoporphyrins, Fractionation, Whole Blood

Evaluating patients with possible diagnoses of erythropoietic protoporphyria or X-linked dominant protoporphyria Establishing a biochemical diagnosis of erythropoietic protoporphyria and X-linked dominant protoporphyria

PIPU - Overview: Pipecolic Acid, Random, Urine

Differentiating between disorders of peroxisomal biogenesis (eg, Zellweger syndrome) and disorders with loss of a single peroxisomal function Detecting abnormal elevations of pipecolic acid in urine

PRSSZ - Overview: PRSS1 Gene, Full Gene Analysis, Varies

Confirmation of suspected clinical diagnosis of hereditary pancreatitis (HP) in patients with chronic pancreatitis Identification of familial PRSSI mutation to allow for predictive and diagnostic testing in family members

FRDIG - Overview: Digoxin, Free, Serum

Evaluating recrudescent (breakthrough) digoxin toxicity in renal-failure patients Assessing the need for more antidigoxin Fab to be administered Deciding when to reintroduce digoxin therapy Monitoring patients with possible...

MPS3W - Overview: Mucopolysaccharidosis III, Four-Enzyme Panel, Leukocytes

Supporting the biochemical diagnosis of mucopolysaccharidoses types IIIA, IIIB, IIIC, IIID This test is not useful for carrier detection.

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.

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).

UPGD - Overview: Uroporphyrinogen Decarboxylase, Whole Blood

Preferred test for the confirmation of a diagnosis of porphyria cutanea tarda type II and hepatoerythropoietic porphyria

SSCTU - Overview: S-Sulfocysteine Panel, Urine

Diagnosis of molybdenum cofactor deficiency, isolated sulfite oxidase deficiency, and hereditary xanthinuria Monitoring patients with molybdenum cofactor deficiency or isolated sulfite oxidase deficiency who are on treatment

YMCRO - Overview: Y Chromosome Microdeletions, Molecular Detection, Varies

Evaluating men with azoospermia, severe oligozoospermia, or otherwise unexplained male factor infertility

IFBA - Overview: Intrinsic Factor Blocking Antibody, Serum

Confirming the diagnosis of pernicious anemia

LYME - Overview: Lyme Disease Serology, Serum

Diagnosing Lyme disease This test should not be used as a screening procedure for the general population. This test should not be used for treatment monitoring.

PIPA - Overview: Pipecolic Acid, Serum

Differentiating between disorders of peroxisomal biogenesis (eg, Zellweger syndrome) and disorders with loss of a single peroxisomal function Detecting abnormal elevations of pipecolic acid in serum

FCLNE - Overview: Anti-Phosphatidylcholine Ab

Anti-Phosphatidylcholine Ab

FPHET - Overview: Anti-Phosphatidylethanolamine Panel

Anti-Phosphatidylethanolamine Panel

FANG1 - Overview: Angiotensin I, Plasma

Angiotensin I, Plasma

FALBU - Overview: Albuterol, Serum/Plasma

Albuterol, Serum/Plasma

FBSQU - Overview: Bath Salts Panel (Qualitative), Urine

Bath Salts Panel (Qualitative), Urine

BOAC - Overview: Boron, Serum/Plasma

Boron, Serum/Plasma

FBAC - Overview: Bile Acids, Urine

Bile Acids, Urine

FBUMT - Overview: Bupropion and Metabolite, Serum

Bupropion and Metabolite, Serum

A1R - Overview: A1 Antigen Subtype, Blood

Additional proof of alloantibody specificity Assessment of solid organ transplantation donor compatibility This test is not useful for the purpose of establishing paternity.

FBART - Overview: Bartonella Antibody Panel, IFA CSF

Bartonella Antibody Panel, IFA CSF

FIFLC - Overview: Immunofixation with Free Light Chains, Quantitative, Urine

Immunofixation with Free Light Chains, Quantitative, Urine

FIN1A - Overview: Interleukin 1-Alpha

Interleukin 1-Alpha

FJCQP - Overview: JC Polyoma Virus DNA, Quantitative Real-Time PCR, Plasma

JC Polyoma Virus DNA, Quantitative Real-Time PCR, Plasma

FCYTP - Overview: Cytokine Panel 13, Serum

Cytokine Panel 13, Serum

FHZCP - Overview: Hazelnut Component Panel

Hazelnut Component Panel

FHTGF - Overview: Human Transforming Growth Factor beta 1 (TGF-b1)

Human Transforming Growth Factor beta 1 (TGF-b1)

FGHSP - Overview: Gamma-Hydroxybutyric Acid (GHB), Serum/Plasma

Gamma-Hydroxybutyric Acid (GHB), Serum/Plasma

FGHRH - Overview: Growth Hormone Releasing Hormone (GH-RH, also known as GHRF or GRF)

Growth Hormone Releasing Hormone (GH-RH, also known as GHRF or GRF)

FHV8P - Overview: Herpesvirus 8 (HHV-8) DNA, Quantitative Real-Time PCR

Herpesvirus 8 (HHV-8) DNA, Quantitative Real-Time PCR

FINA - Overview: NAbFeron (IFNB-1) Neutralizing Antibody Test

Detection of antibodies to interferon-B-1

FNEU2 - Overview: Neurotensin

Neurotensin

FPAIG - Overview: Plasminogen Activator Inhibitor-1, 4G/5G Genotyping (PAI-1 Polymorphism)

Plasminogen Activator Inhibitor-1, 4G/5G Genotyping (PAI-1 Polymorphism)