Hypochondroplasia (FGFR3) Gene Mutation Analysis
von Willebrand Disease 2N (Subtype Normandy), Genotyping
Vasculitis, Systemic
Proteomic Blood Test for Non-Small Cell Lung Cancer (NSCLC), VeriStrat
Hyponatremia
Alzheimer's disease
Lysozyme (Muramidase), Serum
Tangier disease (Familial alpha-lipoprotein deficiency)
Maple Syrup Disease Genetic Testing
Peritoneal Fluid Analysis
LDS
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Tuberculin skin test
All
Diseases
CPT
ICD10
Additional ICD10
All
Diseases
CPT
ICD10
Additional ICD10
Tuberculin skin test
Medical Test
CPT
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Tuberculin skin test
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