Oxygen, Partial Pressure
9p21 Genotype (CVD Risk Genotype Test)
Gestational trophoblastic disease
Amebic infection
Bone Alkaline Phosphatase, Serum
Glomerulonephritis, chronic
Gram Stain, Sputum
Cerebrospinal Fluid Glutamine
Ecstasy, Urine
Hereditary Peripheral Neuropathies Gene Mutation Panel, NGS
LDS
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Peripheral Myelin Protein 22 (PMP22) Gene Mutation Analysis
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
Peripheral Myelin Protein 22 (PMP22) Gene Mutation Analysis
Medical Test
LOINC
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Peripheral Myelin Protein 22 (PMP22) Gene Mutation Analysis
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