Very Long Chain Acyl-CoA Dehydrogenase Deficiency, Gene Mutation Analysis
Ehrlichia chaffeensis Antibody, IgM
Beta-2 Glycoprotein 1 Antibody Panel (IgA, IgG, IgM)
Estrone, Serum
JAK2 Gene Mutation (V617F) Analysis
Ureaplasma species, Molecular
CDKN1C Gene Mutation Analysis
Dopamine transporter (DAT1) (SLC6A3) Genotyping
FibroTest (FibroSURE), Liver Fibrosis Test
Babesia microti, Molecular

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/Nickel, Random, Urine

All
Diseases
CPT
LOINC
ICD10
Additional ICD10

All
Diseases
CPT
LOINC
ICD10
Additional ICD10

Nickel, Random, Urine
Medical Test

Additional ICD10

Access to Nickel, Random, Urine is restricted.