• Vascular Endothelial Growth Factor (VEGF)
  • Chromosome Analysis, Hematologic Disorders, Blood
  • Chronic Fatigue Syndrome Diagnostic Panel
  • N-Acetyltransferase 2 (NAT2) Gene Mutation Analysis
  • Fecal Fat
  • Oncotype DX, Prostate Cancer
  • Parvovirus B19 Antibody, IgG
  • Essential thrombocythemia
  • Tissue Transglutaminase (tTG) Antibody, IgA
  • VDRL Test, CSF
  • LDS
  • Sign up
  • Log in
  • LDS
  • /Medical Tests
  • /Genetic Testing for Severe Inherited Diseases, NGS
  • 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

Genetic Testing for Severe Inherited Diseases, NGS
Medical Test

Interpretation
Access to Genetic Testing for Severe Inherited Diseases, NGS is restricted.