T-Cell Receptor Gene Rearrangement, Flow Cytometry, Bone Marrow
Complete Autoimmune (Connective Tissue Autoimmune) Disease Panel
Hantavirus Antibody, IgG, IgM
Cytochrome P450 2B6 (CYP2B6) Genotyping
Dopamine receptor 1 (DRD1) Genotyping
Neurotrophic Receptor Tyrosine Kinase 3 (NTRK3) Gene Mutation Analysis (Translocation)
Protein, Total, CSF
Human Chorionic Gonadotropin (hCG), Qualitative, Urine
Coagulation Factor VII Activity Assay, Plasma
Thyroid Stimulating Hormone Receptor Antibody (TRAb)
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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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