Metabolic Storage Disease Gene Mutation Panel, NGS
Cyclic Citrullinated Peptide (CCP) Antibody, IgG
Lipase, Serum
Epidermal Nerve Fiber Density (ENFD)
Leucine Aminopeptidase, Serum
UBE3A Gene Mutation Analysis, Angelman Syndrome, Tissue
Activated Clotting Time (ACT)
Clobazam, Urine
Neuron Specific Enolase (NSE), CSF
Secondary hypothyroidism
LDS
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Phenylalanine, Plasma
All
Diseases
CPT
ICD10
Additional ICD10
All
Diseases
CPT
ICD10
Additional ICD10
Phenylalanine, Plasma
Medical Test
ICD10
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Phenylalanine, Plasma
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