Islet Cell (IA-2) Autoantibodies
Multiple Sulfatase Deficiency, Gene Mutation Analysis
Methlyenetetrahydrofolate reductase (MTHFR) Mutation Analysis
Heparin-PF4 Antibody (HIT)
Sodium, Body Fluid
Procainamide, Urine, or Serum
Zinc Finger CCCH-type, RNA Binding Motif and Serine/arginine-rich 2 (ZRSR2) Gene Mutation Analysis
Allergen Specific IgE, Mold (Allergens) Panel
Biopsy, Esophagus
Interleukin 28 B (IL28B) Gene Variation Analysis

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/Amyotrophic Lateral Sclerosis Gene Mutation Panel, NGS

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

Amyotrophic Lateral Sclerosis Gene Mutation Panel, NGS
Medical Test

Additional ICD10

Access to Amyotrophic Lateral Sclerosis Gene Mutation Panel, NGS is restricted.

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