Protoporphyrins, Fractionation, Whole Blood
Chromosome Breakage Study, Bone Marrow
Short-Chain Acyl-CoA Dehydrogenase (SCAD) Deficiency, Genetic Mutation Analysis
Paroxetine, Urine
Angiotensin Converting Enzyme (ACE), Serum/Plasma
CNBP Genetic Analysis for Myotonic Dystrophy, Type II (DM2)
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Tropheryma whipplei, Molecular
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Diseases
Overview
Clinical Utility
Interpretation
Reference Ranges
Methodology
Specimen Collection
Additional Testing
CPT
LOINC
ICD10
Additional ICD10
References
All
Diseases
Overview
Clinical Utility
Interpretation
Reference Ranges
Methodology
Specimen Collection
Additional Testing
CPT
LOINC
ICD10
Additional ICD10
References
Tropheryma whipplei, Molecular
Medical Test
Additional ICD10
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Tropheryma whipplei, Molecular
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