Sodium, 24 Hour, Urine
Fabry (Anderson) disease
Familial Hypercholesterolemia and Related Diseases Multi-Gene Panel, NGS
Lamellar Body Count, Amniotic Fluid
B-Cell Acute Lymphoblastic Leukemia (ALL), FISH, Blood
Familial dysautonomia
UBE3A Gene Mutation Analysis, Angelman Syndrome, Tissue
Gram Stain, Routine
Cancer Antigen (CA) 19-9, Serum
PT and aPTT
LDS
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Prolyl Hydroxylase Domain-2 (PHD2/EGLN1) Gene 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
Prolyl Hydroxylase Domain-2 (PHD2/EGLN1) Gene Mutation Analysis
Medical Test
Additional Testing
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Prolyl Hydroxylase Domain-2 (PHD2/EGLN1) Gene Mutation Analysis
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