Hereditary Hemorrhagic Telangiectasia, ACVRL1 Gene Mutation Analysis
Thyroxine, Free (FT4)
Beta-Glucuronidase, Blood
Cortisol, Salivary
Hepatitis D Virus (HDV) RNA, Molecular Method
Short-Chain Acyl-CoA Dehydrogenase (SCAD) Deficiency, Genetic Mutation Analysis
Solute Carrier Family 28 Member 3 (SLC28A3) Genotyping
Acetylcholine Receptor (AChR) Antibody
MSH6 Gene Mutation Analysis (Known Mutations, Duplication/Deletion/Sequencing)
Biopsy, Testicular
LDS
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Glucose, Cerebrospinal Fluid (CSF)
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Diseases
Overview
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LOINC
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All
Diseases
Overview
Clinical Utility
Interpretation
Reference Ranges
Methodology
Specimen Collection
Additional Testing
Turnaround Time
CPT
LOINC
ICD10
Additional ICD10
References
Glucose, Cerebrospinal Fluid (CSF)
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Diseases (42)
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Overview
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Clinical Utility
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Interpretation
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Reference Ranges
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Methodology
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Specimen Collection
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CPT
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LOINC
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ICD10
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Additional ICD10
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