• Pyruvate, Spinal Fluid
  • Bartonella Antibody, IgG, Serum
  • Micrometastasis Detection
  • Francisella tularensis Antibody, IgM
  • Cryoglobulin, Serum
  • Cytomegalovirus (CMV) Genotyping and Drug Resistance
  • Histoplasma capsulatum Nucleic Acid Detection, Molecular Method
  • HLA C Genotype
  • Nexilin-like Protein (NEXN) Gene Mutation Analysis
  • C1 Esterase Inhibitor, Functional Assay
  • LDS
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  • /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

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