PRSS1 Gene Mutation Analysis
Ureaplasma species, Molecular
Transthyretin (TTR) Gene Mutation Analysis
Prenatal Carrier Screening for Inherited Genetic Conditions (Genesys Carrier Panel, LabCorp Inheritest®, UNITY Fetal Risk screen)
Dopamine beta-hydroxylase (DBH) Genetic Variations
Beta-2 Microglobulin, Serum
Bromide, Serum
Factor II (Prothrombin) Mutation
Fine Needle Aspiration Biopsy and Fine Needle Core Biopsy
Parvovirus B19, Molecular Detection, PCR
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Very Long Chain Acyl-CoA Dehydrogenase Deficiency, Gene Mutation Analysis
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
Very Long Chain Acyl-CoA Dehydrogenase Deficiency, Gene Mutation Analysis
Medical Test
LOINC
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Very Long Chain Acyl-CoA Dehydrogenase Deficiency, Gene Mutation Analysis
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