CNBP Genetic Analysis for Myotonic Dystrophy, Type II (DM2)
Malaria, Molecular Detection, PCR
Lactate Dehydrogenase (LDH), Serum
Complete Autoimmune (Connective Tissue Autoimmune) Disease Panel
Hereditary Hemolytic Anemia Gene Mutation Panel, NGS
Legionella pneumophila Antibody, IgG by IFA
Serine and Arginine-rich Splicing Factor 2 (SRSF2) Gene Mutation Analysis
Copper, 24 Hour, Urine
Beta-Glucuronidase, Fibroblasts
MAML2 (11q21) Rearrangement, Mucoepidermoid Carcinoma (MEC), FISH, Tissue
LDS
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Hydromorphone, Urine
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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
Hydromorphone, Urine
Medical Test
CPT
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Hydromorphone, Urine
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