Chlorpheniramine, Urine
Solute Carrier Family 22 (SLC22A5) Gene Mutation Analysis
Osteocalcin, Serum
Subtelomeric Region Anomalies, FISH, Blood
Lead, Random, Urine
Wilson Disease, (ATP7B) Gene Mutation Analysis
Malignant neoplasm of parathyroid gland (parathyroid carcinoma)
Hereditary Erythrocytosis Gene Mutation Panel, NGS
Estriol, Unconjugated, Serum
PTPN22 Genotype, 1858C->T for Rheumatoid arthritis (RA)
LDS
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Complement Component C3, Serum
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
Complement Component C3, Serum
Medical Test
Additional ICD10
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Complement Component C3, Serum
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