Selenium/Creatinine Ratio, Random, Urine
Prenatal Carrier Screening for Inherited Genetic Conditions (Genesys Carrier Panel, LabCorp Inheritest®, UNITY Fetal Risk screen)
Prolyl Hydroxylase Domain-2 (PHD2/EGLN1) Gene Mutation Analysis
Neurofibromatosis Type 2 (NF2) Gene Mutation Analysis
Vitamin K Epoxide Reductase Complex, Subunit 1 (VKORC1) Genotyping
Hyperthyroidism, primary
Inflammatory Myofibroblastic Tumors (IMT), 2p23 Rearrangement, FISH, Tissue
Toxoplasma IgG
Dexamethasone Suppression Test (Low Dose)
Epidermal Growth Factor Receptor (EGFR), IHC
LDS
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Cytomegalovirus (CMV) Antibody, IgG
All
Diseases
Overview
Clinical Utility
Interpretation
Reference Ranges
Methodology
Specimen Collection
Additional Testing
Turnaround Time
CPT
LOINC
ICD10
Additional ICD10
References
All
Diseases
Overview
Clinical Utility
Interpretation
Reference Ranges
Methodology
Specimen Collection
Additional Testing
Turnaround Time
CPT
LOINC
ICD10
Additional ICD10
References
Cytomegalovirus (CMV) Antibody, IgG
Medical Test
Clinical Utility
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Cytomegalovirus (CMV) Antibody, IgG
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