• Prenatal Carrier Screening for Inherited Genetic Conditions (Genesys Carrier Panel, LabCorp Inheritest®, UNITY Fetal Risk screen)
  • Warfarin Sensitivity (CYP2C9, CYP4F2, VKORC1)
  • Respiratory Viral Pathogen Panel, Molecular
  • Idiopathic Pulmonary Fibrosis Diagnostic Test (Envisiaâ„¢)
  • Protein Immunofixation Electrophoresis, Serum
  • Toxoplasma Gondii IgG and IgM, CSF
  • Mumps Virus Antibody, IgG, IgM
  • Noonan Spectrum Disorders Gene Mutation Panel, NGS
  • Erythropoietin
  • Chlamydia pneumoniae, Culture
  • LDS
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  • /Genetic Testing for Severe Inherited Diseases, NGS
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  • Methodology
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  • CPT
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  • Additional ICD10
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  • 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

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