CNBP Genetic Analysis for Myotonic Dystrophy, Type II (DM2)
Acanthamoeba and Naegleria Culture and Stains, Corneal Scraping
Fragile X, FMR1 Gene Mutation Analysis
Acute intermittent porphyria
Zaleplon, Urine
Ganglioside (GM1, GD1b, and GQ1b) Antibody, IgG and IgM
Prolactin
Vitamin K1
Hemoglobin Electrophoresis
Prostaglandin D2 (PGD2), Serum
LDS
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Trimethoprim, Serum
All
Diseases
CPT
LOINC
ICD10
Additional ICD10
All
Diseases
CPT
LOINC
ICD10
Additional ICD10
Trimethoprim, Serum
Medical Test
CPT
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Trimethoprim, Serum
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