• Norovirus, EIA, Stool
  • Wilson Disease, (ATP7B) Gene Mutation Analysis
  • Alpha-tropomysin (TPM1) Mutation Analysis
  • CaM Kinase II (CaMKII, Calcium-dependent Calmodulin Protein Kinase II) Activation
  • Human Immunodeficiency Virus (HIV) 1 and 2 Western Blot Confirmation Assay
  • Glomerular Filtration Rate, Estimated (eGFR)
  • Carnitine Palmitoyltransferase II Deficiency, Gene Mutation Analysis
  • Influenza Virus Type A, B and Respiratory Syncytial Virus (RSV), PCR
  • Atypical Pneumonia DNA Panel, Sputum
  • Familial Dysautonomia Genetic Mutation Analysis
  • 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

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