• Septin 9 (SEPT9) Methylation Analysis (Epi proColon, ColoVantage)
  • Acute viral encephalitis
  • Glomerulonephritis, acute
  • Complement Component C3A
  • Angiotensin Converting Enzyme (ACE), CSF
  • Measles (Rubeola) Antibody, IgM
  • Helicobacter pylori Antibody, IgA
  • MYOZ2 (Calsarcin-1) Gene Mutation Analysis
  • 1p/19q Deletion in Gliomas, FISH, Tissue
  • Bilirubin Total, Serum
  • LDS
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  • /Lysosomal Storage Disease Gene Mutation Panel, NGS
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  • 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

Lysosomal Storage Disease Gene Mutation Panel, NGS
Medical Test

Methodology
Access to Lysosomal Storage Disease Gene Mutation Panel, NGS is restricted.