• Copper, 24 Hour, Urine
  • Hepatitis B Core Antibody, IgG
  • N-Acetyltransferase 2 (NAT2) Gene Mutation Analysis
  • Products of Conception (POC) Aneuploidy Detection, FISH, Tissue
  • Familial transient neonatal hyperbilirubinemia
  • 2,3-Dinor-11Beta-Prostaglandin F2 Alpha, Urine
  • PIK3CA Gene Mutation Analysis (Therascreen PIK3CA)
  • Chromosome Breakage Study, Blood
  • Carnitine deficiency
  • Follicular Lymphoma, bcl-2/JH t(14;18), FISH
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  • /Severe Combined Immunodeficiency Gene Panel, NGS
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  • 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

Severe Combined Immunodeficiency Gene Panel, NGS
Medical Test

Specimen Collection
Access to Severe Combined Immunodeficiency Gene Panel, NGS is restricted.