Prenatal Carrier Screening for Inherited Genetic Conditions (Genesys Carrier Panel, LabCorp Inheritest®, UNITY Fetal Risk screen)
Amylase, Random, Urine
Hepatitis C Virus (HCV) by Molecular Method, Qualitative or Quantitative
Helicobacter pylori Antigen, Feces
Bullous Pemphigoid, BP180 and BP230, IgG Antibodies
RET/PTC Gene Rearrangement, Molecular
Thiopental, Urine
Protein, Total, Random, Urine
Calcitonin, Fine-Needle Aspiration Biopsy Needle Wash
Coagulation Factor XI Activity Assay, Plasma
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MYOZ2 (Calsarcin-1) Gene Mutation Analysis
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Diseases
Overview
Clinical Utility
Interpretation
Reference Ranges
Methodology
Specimen Collection
Additional Testing
Turnaround Time
CPT
ICD10
Additional ICD10
References
All
Diseases
Overview
Clinical Utility
Interpretation
Reference Ranges
Methodology
Specimen Collection
Additional Testing
Turnaround Time
CPT
ICD10
Additional ICD10
References
MYOZ2 (Calsarcin-1) Gene Mutation Analysis
Medical Test
Diseases (1)
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MYOZ2 (Calsarcin-1) Gene Mutation Analysis
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Overview
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MYOZ2 (Calsarcin-1) Gene Mutation Analysis
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Clinical Utility
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Interpretation
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Reference Ranges
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Methodology
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Specimen Collection
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Additional Testing
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MYOZ2 (Calsarcin-1) Gene Mutation Analysis
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Turnaround Time
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CPT
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LOINC
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ICD10
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Additional ICD10
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References
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Panel Test Components
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