15q Deletion, Type I and Type II Characterization, Prader-Willi/Angelman Syndromes, FISH
Amphetamine, Urine
Ova and Parasites, Stool
Catecholamine Fractionation, Free, 24 Hour, Urine
D-Xylose Absorption Test
Alkaline Phosphatase Isoenzymes
Neuron-Specific Enolase (NSE), Serum
Lipid Panel
GBA, Gaucher Disease Mutation Analysis
The Enhanced Liver Fibrosis (ELF)
LDS
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Short-Chain Acyl-CoA Dehydrogenase (SCAD) Deficiency, Genetic Mutation Analysis
All
Diseases
Overview
Clinical Utility
Interpretation
Reference Ranges
Methodology
Specimen Collection
Additional Testing
Turnaround Time
CPT
ICD10
Additional ICD10
References
All
Diseases
Overview
Clinical Utility
Interpretation
Reference Ranges
Methodology
Specimen Collection
Additional Testing
Turnaround Time
CPT
ICD10
Additional ICD10
References
Short-Chain Acyl-CoA Dehydrogenase (SCAD) Deficiency, Genetic Mutation Analysis
Medical Test
Diseases (1)
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Short-Chain Acyl-CoA Dehydrogenase (SCAD) Deficiency, Genetic Mutation Analysis
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