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1

 

1p/19q Deletion in Oligodendrogliomas
2

 

21-Hydroxylase Deficiency Congenital Adrenal Hyperplasia - 21-OHD CAH
A

 

Acromegaly
Acromegaly Testing Algorithm
Acute Coronary Syndrome - Ischemic Heart Disease
Acute Kidney Injury and Chronic Kidney Disease Testing Algorithm
Acute Lymphoblastic Leukemia - ALL
Acute Lymphoblastic Leukemia FISH Panels
Acute Myeloid Leukemia - AML
Acute Myeloid Leukemia Mutation Panel by Next Generation Sequencing
Acute Pancreatitis
Adalimumab and Antibodies to Adalimumab Quantitation
Adrenal Hyperfunction (Cushing Syndrome) Testing Algorithm
Adrenal Hyperfunction - Cushing Syndrome
Adrenal Insufficiency
Adrenal Insufficiency Testing Algorithm
Alcohol Use Biomarkers
Aldosterone-Renin Ratio
Alloimmune Hemolytic Disease of the Fetus and Newborn (RhCc, RhEe, RhD, or Kell Antigen Genotyping)
Alpha Thalassemia
Alpha-1-Antitrypsin Deficiency Testing
Alpha-Iduronidase Enzyme Activity in Leukocytes
Alport Syndrome Panel, Sequencing and Deletion/Duplication
Alzheimer's Disease
Alzheimer’s Disease Markers, CSF
Amenorrhea
Amenorrhea Testing Algorithm
Analytical Considerations in the Evaluation of Thyroid Function
Anemia
Anemia of Chronic Disease - Anemia of Inflammation
Anemia Testing Algorithm
Anemias and Hemoglobinopathies
Angelman Syndrome and Prader-Willi Syndrome
Angelman Syndrome and Prader-Willi Syndrome by Methylation-Specific MLPA
Ankylosing Spondylitis (HLA-B27) Genotyping
Antiglomerular Basement Membrane Disease - Goodpasture Syndrome
Antinuclear Antibody (ANA) With HEp-2 Substrate
Antinuclear Antibody Disease Testing Algorithm
Antinuclear Antibody Disease Testing Algorithm - Cytoplasmic Patterns
Antinuclear Antibody Disease Testing Algorithm - Nuclear Patterns
Antiphospholipid Syndrome - APS
Antiphospholipid Syndrome Reflex Panel
Antiphospholipid Syndrome Testing Algorithm
Aortopathy Panel, Sequencing and Deletion/Duplication
APC- and MUTYH-Associated Polyposis Panel, Sequencing and Deletion/Duplication
Apolipoprotein E (APOE) Genotyping, Alzheimer Disease Risk
Apolipoprotein E Genotyping, Cardiovascular Disease Risk
ARUP Consult Editorial Board
ARUP Consult Redesign FAQs
ARUP Estrogen Tests Comparison
ARUP Free or Bioavailable Testosterone Test Options (Adult Females, Children, or Individuals on Testosterone-Suppressing Hormone Therapy)
ARUP Free or Bioavailable Testosterone Test Options (Adult Males or Individuals on Testosterone Hormone Therapy)
ARUP Immunobullous Disease Testing Comparison
ARUP Testosterone Tests Comparison
Ashkenazi Jewish Genetic Diseases
Ashkenazi Jewish Genetic Diseases Panel
Atherosclerotic Cardiovascular Disease Risk Assessment
ATI Removal Notification
Autism and Intellectual Disability Comprehensive Panel
Autoimmune CNS Demyelinating Disease Reflexive Panel
Autoimmune Dysautonomia Panel, Serum
Autoimmune Encephalitis
Autoimmune Encephalopathy and Dementia Panel, Serum and CSF
Autoimmune Epilepsy Panel, Serum and CSF
Autoimmune Hepatitis
Autoimmune Liver Disease Testing Algorithm
Autoimmune Movement Disorder Panel, Serum and CSF
Autoimmune Myelopathy Panel, Serum and CSF
Autoimmune Neurologic Disease Panel With Reflex, Serum and CSF
Autoimmune Neurologic Diseases - Antineural Antibody Testing
Autoimmune Neuromuscular Junction Reflexive Panel
Autoimmune Neuropathies - Neuropathic Disease
Autoimmune Pediatric CNS Disorders Panel, Serum and CSF
Autoimmune Stiff-Person Disorders Panel, Serum and CSF
Autoimmune Thyroiditis
Autoimmune Vision Loss Panel, Serum
B

 

B-Cell Acute Lymphoblastic Leukemia Minimal Residual Disease Detection by Flow Cytometry
Bariatric Surgery - Nutritional Assessment
Bartonella Infection
BCR-ABL1 (BCR::ABL1) Qualitative and Quantitative Testing
BCR-ABL1 Mutation Analysis for Tyrosine Kinase Inhibitor Resistance
Beckwith-Wiedemann and Russell-Silver Syndromes
Benzodiazepine Metabolism Diagram
Beta Globin (HBB) Sequencing
Biotinidase Deficiency
Biotinidase Deficiency (BTD) Sequencing
Birt-Hogg-Dubé Syndrome
Bladder Cancer
Bordetella pertussis - Whooping Cough
Borrelia burgdorferi Antibodies With Reflex to ELISA
BRAF Mutation Detection
Breast Cancer Biomarkers
Brucella Species - Brucellosis
C

 

C1-INH Deficiency Testing Algorithm
C1q Antibody, IgG
Calprotectin, Fecal by Immunoassay
Capillary Malformation-Arteriovenous Malformation
Cardiomyopathy and Arrhythmia Panel, Sequencing and Deletion/Duplication
Cardiovascular Genetic Testing - Hereditary Heart and Vascular Disease
Carrier Screening for Genetic Disorders
Celiac Disease
Celiac Disease HLA-DQ Genotyping
Celiac Disease Reflexive Cascade, Serum
Central Diabetes Insipidus (Posterior Pituitary) Testing Algorithm
Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy, CADASIL (NOTCH3), Sequencing
Cerebral Cavernous Malformation Panel, Sequencing and Deletion/Duplication
Cerebrospinal Fluid (CSF) Leak
Cervical Cancer Screening: 25 to 65 Years of Age
Cervical Cancer Screening: Older Than 65 Years
Cervical Cancer Screening: Younger Than 25 Years
Charcot-Marie-Tooth Disease and Related Hereditary Neuropathies
Chimerism Testing by Short Tandem Repeat (STR) Genotyping
Chromogenic Factor VIII, Activity
Chronic Hepatitis B Virus Testing Algorithm
Chronic Lymphocytic Leukemia - CLL
Chronic Lymphocytic Leukemia Minimal Residual Disease Detection by Flow Cytometry
Chronic Lymphocytic Leukemia Mutation Panel by Next Generation Sequencing
Chronic Myeloid Leukemia - CML
Chronic Pancreatitis
Classic 21-Hydroxylase Deficiency Congenital Adrenal Hyperplasia Testing
Classic Galactosemia
Clinical Toxicology Testing
Clostridioides (Clostridium) difficile
Clostridioides (Clostridium) difficile Infection Testing Algorithm
Cobalamin/Propionate/Homocysteine Metabolism-Related Disorders Panel
Colorectal (Colon) Cancer
Colorectal Cancer Mutation Panel
Common Variable Immunodeficiency
Community-Acquired Pneumonia - CAP
Complement Deficiency Testing Algorithm
Complement Testing - Complement Deficiency and Anticomplement Therapeutic Response Monitoring
Comprehensive Epilepsy Panel, Sequencing and Deletion/Duplication
Connective Tissue Diseases - Systemic Autoimmune Rheumatic Diseases
COVID-19 - SARS-CoV-2
Coxiella burnetii - Q Fever
Creatine Disorders Panel Testing
CSF Bilirubin in Subarachnoid Hemorrhage
CYFRA 21-1 (Cytokeratin 19 Fragment) in Lung Cancer
Cystic Fibrosis
Cystic Fibrosis (CFTR) Expanded Variant Panel
Cystic Fibrosis (CFTR) Sequencing and Deletion/Duplication
Cytochrome P450 Genotyping
Cytogenomic Microarray, Oncology
Cytogenomic Microarray, Products of Conception
Cytogenomic SNP Microarray
Cytogenomic SNP Microarray, Fetal
Cytomegalovirus - CMV
D

 

Deep Vein Thrombosis Testing Algorithm
Dengue, West Nile, and Other Mosquito-Borne Arboviruses
Dermatitis Herpetiformis
Dermatomyositis and Polymyositis Panel
Dermatomyositis Autoantibody Panel
Diabetes Mellitus - Type 1, Type 2, and Gestational
Diabetes-Associated Autoantibodies
Dihydropyrimidine Dehydrogenase (DPYD) and UPD Glucuronosyltransferase 1A1 (UGT1A1) Genotyping
Dihydropyrimidine Dehydrogenase (DPYD), 3 Variants
Dilated Cardiomyopathy Panel, Sequencing
Direct Xa Inhibitor Levels
Disclaimer
Disseminated Intravascular Coagulation - DIC
Distal Arthrogryposis Panel
Drug Detection Panel Testing, Meconium and Umbilical Cord Tissue
Drug Half-Lives and Urine Detection Windows
Drug Profile, Expanded Targeted Panels
Drug Profiles, Targeted by Mass Spectrometry and Enzyme Immunoassay
Drug Testing
Duchenne/Becker Muscular Dystrophy Deletion/Duplication With Reflex to Sequencing
E

 

Early-Onset Alzheimer's Panel, Sequencing
Echinococcus Species - Echinococcosis Infection
Editorial Policy
Emergency Toxicology
Emery-Dreifuss Muscular Dystrophy Panel, Sequencing
Endocrine Testing in Transgender Adults
Eosinophil-Related Disorders - Eosinophilia
Eosinophil-Related Disorders Testing Algorithm
Epidermolysis Bullosa Acquisita
Epstein-Barr Virus - EBV
ERBB2 (HER2/neu) (HercepTest) Testing
Ethyl Glucuronide, Umbilical Cord Tissue, Qualitative
Evaluation of Acute Kidney Injury and Chronic Kidney Disease
Evaluation of Infertility
Evaluation of Liver Function
Exome Sequencing
Extended Myositis Panel
F

 

Factor V Leiden (F5) R506Q Variant
Factor XIII Deficiency Testing
Familial Hypercholesterolemia Panel, Sequencing
Familial Mediterranean Fever (MEFV) Sequencing
Familial Transthyretin Amyloidosis (TTR) Sequencing
Fatty Acid Oxidation Disorders Panel, Sequencing
Fibrinolytic Disorders
Fragile X (FMR1) With Reflex to Methylation Analysis
Fragile X (FMR1)-Associated Disorders
Frequently Asked Questions
Functional Platelet Disorders
G

 

Galactosemia Genetic Testing
Gamma Globin (HBG1 and HBG2) Sequencing
Gastrointestinal Stromal Tumors (GISTs)
Gaucher Disease
Genetic Carrier Screen (CF, FXS, and SMA) With Reflex to Methylation
Genital Ulcer Disease Panel
Germline Pharmacogenetics - PGx
Gestational Trophoblastic Disease
Glucagonoma
Glucose-6-Phosphate Dehydrogenase (G6PD) Deficiency by DNA
Glycogen Storage Disorders Panel, Sequencing
Gout
Group A Streptococcal Disease - Strep Throat
Group B Streptococcal Disease
Growth Hormone Deficiency
Growth Hormone Testing in Adult Patients Testing Algorithm
Growth Hormone Testing in Pediatric Patients Testing Algorithm
Growth Hormone Testing in Transition Patients Testing Algorithm
H

 

Heart Failure
Helicobacter pylori
Helicobacter pylori Testing Algorithm
Hematologic Malignancies
Hemochromatosis
Hemochromatosis (HFE) 3 Variants
Hemochromatosis Testing Algorithm
Hemoglobin Evaluation Reflexive Cascade
Hemoglobinopathies
Hemoglobinopathies Testing Algorithm
Hemolytic Anemias
Hemolytic Anemias Testing Algorithm
Hemolytic Disease of the Fetus and Newborn
Hemophilia - Factor VIII or IX Deficiency
Hemophilia A (F8) Genetic Testing
Hemostasis and Thrombosis Testing
Heparin-Induced Thrombocytopenia - HIT
Hepatocellular Carcinoma Serum Markers
Hereditary Bone Marrow Failure Panel, Sequencing and Deletion/Duplication
Hereditary Breast and Gynecologic Cancers Panel
Hereditary Breast Cancer Panels (Including BRCA1 and BRCA2)
Hereditary Cancer Germline Genetic Testing
Hereditary Cancer Panel
Hereditary Central Nervous System Cancer Panel, Sequencing and Deletion/Duplication
Hereditary Coenzyme Q Deficiency Syndromes - Ubiquinone Deficiency
Hereditary Erythrocytosis Panel, Sequencing
Hereditary Gastric Cancer Panel, Sequencing and Deletion/Duplication
Hereditary Gastrointestinal Cancer Panels
Hereditary Hearing Loss
Hereditary Hearing Loss - GJB2 and GJB6 Testing
Hereditary Hemolytic Anemia Cascade
Hereditary Hemolytic Anemia Panel, Sequencing
Hereditary Hemorrhagic Telangiectasia - HHT
Hereditary Hemorrhagic Telangiectasia Panel
Hereditary Melanoma Panel, Sequencing and Deletion/Duplication
Hereditary Myeloid Neoplasms Panel, Sequencing
Hereditary Pancreatic Cancer Panel, Sequencing and Deletion/Duplication
Hereditary Paraganglioma-Pheochromocytoma Panels
Hereditary Prostate Cancer Panel, Sequencing and Deletion/Duplication
Hereditary Renal Cancer Panel
Hereditary Retinoblastoma (RB1) Sequencing and Deletion/Duplication
Hereditary Thrombophilia - Hypercoagulability
Hereditary Thyroid Cancer Panel, Sequencing and Deletion/Duplication
Herpes Simplex Virus - HSV
Heterotaxy and Situs Inversus Panel
HIV Testing in Adults and Adolescents Algorithm
HLA Testing
HLA-B*15:02 Genotyping, Carbamazepine Hypersensitivity
HLA-B*57:01 for Abacavir Sensitivity
HLA-B*58:01 Genotyping, Allopurinol Hypersensitivity
Holoprosencephaly Panel, Sequencing and Deletion/Duplication
Hospital-Acquired and Ventilator-Associated Pneumonia
Human Immunodeficiency Virus - HIV
Human Papillomavirus
Huntington Disease
Huntington Disease (HD) CAG Repeat Expansion
Hypercalcemia and Hypocalcemia - Vitamin D Testing
Hypercalcemia Testing Algorithm
Hypertrophic Cardiomyopathy Panel, Sequencing
Hypocalcemia Testing Algorithm
Hypogonadism Testing Algorithm
Hypopituitarism
Hypopituitarism (Anterior Pituitary) Testing Algorithm
Hypothyroidism
I

 

IDH1-IDH2 Mutation Detection
IgG4-Related Disease
Immunization Status
Immunobullous Diseases Testing Algorithm - Epithelial Antibody Associated
Immunobullous Diseases Testing Algorithm - Neoplastic Disease
Immunobullous Diseases Testing Algorithm - Pregnancy
Immunobullous Diseases, Epithelial Antibody Associated
Impacts of Common Anticoagulants on Coagulation Testing
Infectious Diarrhea
Infectious Diarrhea Testing Algorithm
Infertility Testing for the Female Reproductive Partner
Infertility Testing for the Male Reproductive Partner
Inflammatory Bowel Disease - IBD
Inflammatory Markers
Inflammatory Myopathies
Infliximab and Antibodies to Infliximab Quantitation
Influenza Virus
Initial Evaluation of Thyroid Function
Insulinoma
Interstitial Lung Disease Autoantibody Panel
Interstitial Lung Diseases
IRF4/DUSP22 Gene Rearrangement by FISH
Iron Deficiency Anemia
Iron Deficiency Anemia and Anemia of Chronic Disease/Anemia of Inflammation Testing Algorithm
J

 

JAK2 (V617F) Mutation by ddPCR
K

 

KIT Molecular Testing
Kratom, Umbilical Cord Tissue, Qualitative
L

 

Laboratory Testing for Developmental Delay, Intellectual Disability, and Autism Spectrum Disorder
Laboratory Testing for Monoclonal Antibody Therapeutics
Laboratory Testing for Neurologic Conditions
Laboratory Testing in Reproductive Medicine
Legionella - Pontiac Fever and Legionnaires Disease
Leukemia/Lymphoma Phenotyping Evaluation by Flow Cytometry
Linear IgA Disease
Loeys-Dietz Syndrome Core Panel, Sequencing
Long QT Panel, Sequencing and Deletion/Duplication
Lung Cancer Mutation Panel
Lupus Anticoagulant Reflex Panel
Lyme Disease - Modified Two-Tiered Testing Algorithm
Lynch Syndrome (HNPCC) Testing Algorithm
Lynch Syndrome - Hereditary Nonpolyposis Colorectal Cancer (HNPCC)
Lynch Syndrome Panel, Sequencing and Deletion/Duplication
M

 

Male Hypogonadism
Malignant Hyperthermia Panel, Sequencing
Marfan Syndrome (FBN1) Sequencing and Deletion/Duplication
Mast Cell Disorders
Mast Cell Disorders Testing Algorithm
Maternal Serum Screening
Mature B-Cell Lymphomas
Maturity-Onset Diabetes of the Young and Neonatal Diabetes Panel, Sequencing
Measles - Rubeola
Medium Chain Acyl-CoA Dehydrogenase (ACADM) 2 Mutations
Megaloblastic Anemia
Megaloblastic Anemia Testing Algorithm
Melanoma
Melanoma Mutation Panel
Methylenetetrahydrofolate Reductase (MTHFR) Testing
Microcytic Anemia Testing Algorithm
Minimal Residual Disease Testing
Mitochondrial Diseases
Mixed Connective Tissue Disease - MCTD
Monitoring of Gender-Affirming Hormone Therapy Testing Algorithm
Monkeypox Virus - Mpox
Multiple Endocrine Neoplasia Type 1 (MEN1) Sequencing and Deletion/Duplication
Multiple Endocrine Neoplasia Type 2, RET Sequencing
Multiple Endocrine Neoplasias - MEN
Multiple Myeloma Minimal Residual Disease Detection by Flow Cytometry
Multiple Myeloma Panel by FISH
Multiple Sclerosis
Mumps Virus
Myasthenia Gravis - MG
Myasthenia Gravis Testing
Mycobacterium tuberculosis - Tuberculosis
MYD88 L265P Mutation Detection by PCR, Quantitative
Myelodysplastic Syndromes
Myeloid Malignancies Mutation and Copy Number Variation Panel by Next Generation Sequencing
Myeloproliferative Neoplasms - MPNs
Myotonic Dystrophy Type 1 (DMPK)
N

 

Neonatal Alloimmune Thrombocytopenia - NAIT
Neonatal Sepsis - Sepsis in Newborns
Nephrolithiasis - Kidney Stone Disease
Nephrolithiasis Testing Algorithm
Neuroblastoma
Neurofibromatosis Type 1 and Legius Syndrome Panel, Sequencing and Deletion/Duplication
Neuromyelitis Optica Spectrum Disorders
Newborn Drug Screening - Meconium and Umbilical Cord Tissue
Newborn Drug Testing Algorithm
Nicotine Exposure and Metabolites
Non-Small Cell Lung Cancer Molecular Markers
Nonclassic 21-Hydroxylase Deficiency Congenital Adrenal Hyperplasia Testing
Noninvasive Prenatal Aneuploidy Screen by Cell-Free DNA Sequencing
Noonan Spectrum Disorders Panel
O

 

Opiates and Opioid Metabolism Diagram
Opioid Receptor, mu OPRM1 Genotype, 1 Variant
Osteogenesis Imperfecta and Low Bone Density Panel, Sequencing
Osteoporosis - Bone Turnover Markers
Ovarian Cancer Biomarkers
P

 

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Pancreatic Neuroendocrine Tumors - PNETs
Pancreatitis Panel
Paraneoplastic Pemphigus
Paraneoplastic Reflexive Panel, Serum and CSF
Paroxysmal Nocturnal Hemoglobinuria - PNH
Paroxysmal Nocturnal Hemoglobinuria Testing
PD-L1 by Immunohistochemistry
PD-L1 Testing
Pemphigoid
Pemphigoid Gestationis - Gestational Pemphigoid
Pemphigus
Periodic Fever Syndromes Panel, Sequencing and Deletion/Duplication
Peroxisomal Disorders Panel, Sequencing
Pharmacogenetics Panel for Psychotropics
Pheochromocytoma - Paraganglioma
Pheochromocytoma - Paraganglioma Biochemical Testing Algorithm
Plasma Cell Dyscrasias
Plasma Cell Dyscrasias Testing Algorithm
Plasminogen Activator Inhibitor-1 (SERPINE1) Genotyping
Plasmodium Species - Malaria
Platelet Antigen Genotyping Panel
Pneumonia Panel by PCR
Polycystic Ovary Syndrome - PCOS
Polycystic Ovary Syndrome in Adolescents Testing Algorithm
Polycystic Ovary Syndrome in Adults Testing Algorithm
Polymyositis Panel
Porphyrias
Porphyrias Testing Algorithm
Preeclampsia Testing
Pregnancy and Prenatal Laboratory Testing
Prenatal Testing for Chromosomal Abnormalities and Neural Tube Defects
Primary Aldosteronism
Primary Aldosteronism Testing Algorithm
Primary Antibody Deficiency Panel, Sequencing and Deletion/Duplication
Primary Biliary Cholangitis - PBC
Primary Brain Tumors – Brain Tumor Molecular Markers
Primary Ciliary Dyskinesia Panel
Primary Immunodeficiency Diseases - Immunoglobulin Disorders
Primary Membranous Nephropathy - Idiopathic Membranous Glomerulonephritis
Primary Membranous Nephropathy Comprehensive Autoantibody Panel
Primary Sclerosing Cholangitis – PSC
Prolonged Clot Time Reflexive Profile
Prolonged Clotting Time Evaluation
Prostate Cancer
Prostate Cancer Early Detection Screening Algorithm
Prothrombin (F2) c.*97G>A (G20210A) Pathogenic Variant
Pulmonary Arterial Hypertension Panel, Sequencing and Deletion/Duplication
Pulmonary Embolism Testing Algorithm
R

 

Rapid Acute Myeloid Leukemia Targeted Therapy Mutation Panel
RBC Band 3 Protein Reduction in Hereditary Spherocytosis
Red Blood Cell Antigen Genotyping
Respiratory Pathogen Molecular Panel Testing
Respiratory Syncytial Virus - RSV
Respiratory Viruses
Rheumatoid Arthritis - RA
Rickettsia typhi - Typhus Fever
Rubella - German Measles
S

 

Schistosoma Species - Schistosomiasis
Sepsis
Septic Arthritis
Sexually Transmitted Infections
SHOX Deficiency Disorders, Sequencing and Deletion/Duplication
Shwachman-Diamond Syndrome
Sjögren Syndrome
Skeletal Dysplasia Panel, Sequencing and Deletion/Duplication
Skeletal Dysplasias
Soft Tissue Sarcomas
Solid Tumor Mutation Panel, Sequencing
Soluble Mesothelin-Related Peptides (MESOMARK)
Somatostatinoma
Spinal Muscular Atrophy Copy Number Analysis
Stickler Syndrome Panel, Sequencing
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Succinylacetone, Quantitative, Urine – Tyrosinemia Type 1
Symptomatic Celiac Disease Testing Algorithm
Syphilis Testing Algorithm
Systemic Lupus Erythematosus - SLE
Systemic Sclerosis - Scleroderma
T

 

T-Cell and NK-Cell Lymphomas
Taenia solium - Cysticercosis and Taeniasis
Tay-Sachs Disease (HEXA) Sequencing and Deletion/Duplication
Testing for Genetic Syndromes Related to Autism Spectrum Disorder (ASD)
Testing for Genetic Syndromes Related to Developmental Delay (DD) and Intellectual Disability (ID)
TFE3 (Xp11.2) Gene Rearrangement by FISH
Thalassemias
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Therapeutic Drug Monitoring - TDM
Thiopurine Metabolites in Red Blood Cells
Thiopurine Methyltransferase, RBC
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Thrombocytopenic Disorders
Thrombotic Microangiopathies - Thrombotic Thrombocytopenic Purpura and Hemolytic Uremic Syndrome
Thrombotic Risk Reflex Panel
Thyroid Cancer
Thyroid Cancer Monitoring and Surveillance Algorithm
Thyroid Cancer Testing Algorithm
Thyroid Disease in Pregnancy
Thyroid Disease Testing
Thyroid Disease Testing Algorithm
Thyroid Nodules
Thyroid Nodules Testing Algorithm
Thyrotoxicosis - Hyperthyroidism
Tickborne Diseases
Toll-Like Receptor Function Testing
Toxocara Species - Toxocariasis
Toxoplasma gondii - Toxoplasmosis
Toxoplasmosis Serologic Testing for Pregnant Individuals Algorithm
TPMT and NUDT15
TPSAB1 Copy Number Analysis by ddPCR
Trace Elements - Deficiency and Toxicity
Treponema pallidum - Syphilis
Trypanosoma cruzi - Chagas Disease
Tuberous Sclerosis Complex Panel, Sequencing and Deletion/Duplication
U

 

UGT1A1 Gene Analysis
Uncommon Factor Deficiencies
Unstable Hemoglobinopathies
Urine Drug Testing (Unexpected Results) Algorithm
Urticaria-Inducing Activity and Urticaria-Induced Basophil Activation
V

 

Vaginitis - Bacterial Vaginosis, Vulvovaginal Candidiasis, and Trichomoniasis
Vaginitis Panel by TMA
Varicella-Zoster Virus - VZV
Vascular Malformations Panel, Sequencing and Deletion/Duplication
Vasoactive Intestinal Polypeptide Secreting Tumor - VIPoma
Venous Thromboembolism
Very Long-Chain Acyl-CoA Dehydrogenase (ACADVL) Deficiency
Very Long-Chain and Branched-Chain Fatty Acids Profile
Viral Hepatitis
Viral Hepatitis Screening and Diagnosis Algorithm
Vitamins - Deficiency and Toxicity
Von Willebrand Disease (VWF) Sequencing
Von Willebrand Disease - VWD
Von Willebrand Disease Testing Algorithm
W

 

Warfarin Sensitivity (CYP2C9, CYP2C cluster, CYP4F2, VKORC1) Genotyping
Whole Genome Sequencing
Wilson Disease
Wilson Disease (ATP7B) Sequencing
Wilson Disease Testing Algorithm
X

 

X-Chromosome Inactivation Analysis
X-Linked Adrenoleukodystrophy
Y

 

Y Chromosome Microdeletions
Z

 

Zollinger-Ellison Syndrome - Gastrinoma
Zollinger-Ellison Syndrome Testing Algorithm