MyoMarker 3 Plus Profile for Idiopathic Inflammatory Myopathies
Human Chorionic Gonadotropin (hCG), Qualitative, Urine
Coagulation Factor VII Activity Assay, Plasma
Thyroid Stimulating Hormone Receptor Antibody (TRAb)
Neisseria gonorrhoeae, Culture
Serine and Arginine-rich Splicing Factor 2 (SRSF2) Gene Mutation Analysis
Delta-type Opioid Receptor 1 (OPRD1) Genotyping
Neisseria gonorrhoeae Ciprofloxacin Susceptibility Testing, PlexPrime GC+gyrA(550)
Apolipoprotein B (APOB) Mutation Detection
Aluminum, Random, 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
Diseases (5)
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Carbohydrate Deficient Transferrin for Congenital Disorders of Glycosylation, Serum
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