1p36.3 Microdeletion Syndrome, FISH
Multiple endocrine neoplasia, type III
Aminolevulinic Acid, Urine
Viral hepatitis
Cystatin C with Estimated GFR, Serum
Prader-Willi and Angelman Syndrome Molecular Analysis
Muscular Dystrophies Gene Mutation Panel, NGS
ASXL1 Gene Mutation Analysis
Medium-Chain Acyl-CoA Dehydrogenase (MCAD) Mutation Analysis
Osteochondritis dissecans

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LDS
/Medical Tests
/Cytochrome P450 21A2 (CYP21A2) Genotyping

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

Cytochrome P450 21A2 (CYP21A2) Genotyping
Medical Test

Access to Cytochrome P450 21A2 (CYP21A2) Genotyping is restricted.