• Cortisol, Total, Urine
  • Hereditary Hemorrhagic Telangiectasia, ACVRL1 Gene Mutation Analysis
  • Angiotensin I, Plasma
  • Prostaglandin D2 (PGD2), Serum
  • Chloride, 24 Hour, Urine
  • Wolf-Hirschhorn Syndrome, 4p16.3 Deletion
  • HDL Cholesterol Subclasses
  • Ehrlichia chaffeensis and Anaplasma Species by Real-Time PCR
  • Hepatitis B Core Antibody, IgG
  • Steroid Sulfatase Gene, Xp22.3 Deletion, FISH
  • LDS
  • Sign up
  • Log in
  • LDS
  • /Medical Tests
  • /Niemann-Pick Disease, Types A and B, Gene Mutation Analysis
  • 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

Niemann-Pick Disease, Types A and B, Gene Mutation Analysis
Medical Test

Clinical Utility
Access to Niemann-Pick Disease, Types A and B, Gene Mutation Analysis is restricted.
Loading...