Potassium, Random, Urine
B and T Cell Gene Rearrangement, Blood
Benztropine, Serum
Thyroglobulin, Fine Needle Aspiration (FNA)
RTEL1 Gene Mutation Analysis
Thyroxine Index, Free
Ehrlichia chaffeensis Antibody, IgM
Mycobacterial Culture, Body Fluid
Carnitine Palmitoyltransferase II Deficiency, Gene Mutation Analysis
Solute Carrier Family 28 Member 3 (SLC28A3) Genotyping
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X-Linked Adrenoleukodystrophy (ABCD1) Gene Mutation Analysis, Blood
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
X-Linked Adrenoleukodystrophy (ABCD1) Gene Mutation Analysis, Blood
Medical Test
Interpretation
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X-Linked Adrenoleukodystrophy (ABCD1) Gene Mutation Analysis, Blood
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