Mucopolysaccharidosis type II (Hunter Syndrome)
von Willebrand Disease 2N (Subtype Normandy), Genotyping
Autoimmune hemolytic anemia
Methicillin resistant Staphylococcus aureus infection
Cytomegalovirus infection
Carcinoembryonic Antigen (CEA), Pancreatic Cyst Fluid
Comprehensive Pharmacogenetics (PGx) Gene Variation Panel
Charcot-Marie-Tooth Disease
Oncotype DX, Breast Cancer
Huntington disease
LDS
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Cotinine, Urine
All
Diseases
Overview
Clinical Utility
Interpretation
Reference Ranges
Methodology
Specimen Collection
Additional Testing
Turnaround Time
CPT
LOINC
ICD10
Additional ICD10
References
All
Diseases
Overview
Clinical Utility
Interpretation
Reference Ranges
Methodology
Specimen Collection
Additional Testing
Turnaround Time
CPT
LOINC
ICD10
Additional ICD10
References
Cotinine, Urine
Medical Test
Additional ICD10
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Cotinine, Urine
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