• Biopsy, Head and Neck
  • Dihydrocodeine, Urine
  • Friedreich Ataxia Repeat Expansion, FXN (frataxin) Gene Analysis
  • Electron Microscopy
  • Noonan Spectrum Disorders Gene Mutation Panel, NGS
  • Aspergillus DNA, Qualitative, Real-Time PCR, Sputum
  • Tangier disease (Familial alpha-lipoprotein deficiency)
  • Tissue Transglutaminase (tTG) Antibody, IgA, IgG
  • Mycoplasma pneumoniae Antibody, IgG
  • Protein, Total, Serum
  • LDS
  • Sign up
  • Log in
  • LDS
  • /Medical Tests
  • /Hypertrophic Cardiomyopathy Gene Mutation Panel, NGS
  • All
  • 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

Hypertrophic Cardiomyopathy Gene Mutation Panel, NGS
Medical Test

CPT
Access to Hypertrophic Cardiomyopathy Gene Mutation Panel, NGS is restricted.