Branched-Chain Amino Acids for Maple Syrup Disease Monitoring
Multiple Endocrine Neoplasia Type 1 (MEN1) Mutation Analysis
Chlordiazepoxide, Serum
Biopsy, Bile Duct
Tumor Necrosis Factor Receptor-Ass Periodic Syndrome (TNFRSF1A) Gene Mutation Analysis
India Ink Preparation, CSF
EarlyTect® Bladder Cancer Detection Test (PENK Gene Methylation Assay)
Cytochrome P450 2B6 (CYP2B6) Genotyping
Hepatitis B Surface Antibody, Quantitative
UDP Glucuronosyltransferase 2B15 (UGT2B15) Genotyping

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/Comprehensive Mitochondrial Disorders Gene Analysis Panel, NGS (Genomic Unity®)

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

Comprehensive Mitochondrial Disorders Gene Analysis Panel, NGS (Genomic Unity®)
Medical Test

Specimen Collection

Access to Comprehensive Mitochondrial Disorders Gene Analysis Panel, NGS (Genomic Unity®) is restricted.