Blood Culture (Bloodstream Infection) Pathogen and Resistance Gene Panel, Molecular
Calcium Channel Voltage-dependent L Type alpha 1S Subunit (CACNA1S) Gene Mutation Analysis
Krabbe Disease (GALC) Gene Mutation Analysis
Alpha Fetoprotein (AFP), Spinal Fluid
Thyroid Stimulating Hormone Receptor Antibody (TRAb)
Neisseria gonorrhoeae Ciprofloxacin Susceptibility Testing, PlexPrime GC+gyrA(550)
Alpha Globin (HBA1 and HBA2) Gene Analysis
MYL3 Gene Mutation Analysis
Hemosiderin Stain, Urine
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Carbohydrate Deficient Transferrin for Congenital Disorders of Glycosylation, Serum
All
Diseases
CPT
LOINC
ICD10
Additional ICD10
All
Diseases
CPT
LOINC
ICD10
Additional ICD10
Carbohydrate Deficient Transferrin for Congenital Disorders of Glycosylation, Serum
Medical Test
ICD10
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Carbohydrate Deficient Transferrin for Congenital Disorders of Glycosylation, Serum
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