• Culture, Acid-Fast Bacilli, Bronchoalveolar Lavage
  • Triglycerides, Serum
  • Prealbumin (Transthyretin)
  • Urea Nitrogen (BUN), Random, Urine
  • Phenobarbital, Serum
  • Lysosomal Acid Lipase, Enzyme Activity
  • Rheumatoid Factor (RF)
  • Nucleophosmin (NPM1) Gene Mutation Analysis
  • Cyclic AMP, Plasma
  • Rubella Antibody, IgG
  • LDS
  • Sign up
  • Log in
  • LDS
  • /Medical Tests
  • /Hypochondroplasia (FGFR3) 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

Hypochondroplasia (FGFR3) Gene Mutation Analysis
Medical Test

ICD10
Access to Hypochondroplasia (FGFR3) Gene Mutation Analysis is restricted.
Loading...