Digoxin, Total, Serum
Carbamazepine, Free and Total, Serum
Kallmann Syndrome, Xp22.3 Deletion, FISH
B-Type Natriuretic Peptide (BNP) or Pro B-Type Natriuretic Peptide (Pro BNP)
Biopsy, Colon
Malignant neoplasm, renal pelvis (kidney)
Synovial Sarcoma, SS18 Gene Translocation, RT-PCR, Paraffin
Amitriptyline, Urine
Amino Acids Quantitative by LC-MS/MS, Plasma
Heparin Antifactor Xa Assay

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LDS
/Medical Tests
/Hereditary Hemochromatosis (HFE) Mutation Assay

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

Hereditary Hemochromatosis (HFE) Mutation Assay
Medical Test

Access to Hereditary Hemochromatosis (HFE) Mutation Assay is restricted.