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
Benign neoplasm, ovary

LDS
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LDS
/Medical Tests
/Selenium/Creatinine Ratio, Random, Urine

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

Selenium/Creatinine Ratio, Random, Urine
Medical Test

Additional Testing

Access to Selenium/Creatinine Ratio, Random, Urine is restricted.