• Peripheral Myelin Protein 22 (PMP22) Gene Mutation Analysis
  • Polyoma BK Virus, PCR, Quantitative, Plasma
  • Aspergillus (Galactomannan) Antigen, Serum
  • Blastomyces Antibody, Spinal Fluid
  • Hereditary Hemorrhagic Telangiectasia, Gene Mutation Panel
  • Pheniramine, Urine
  • Apolipoprotein Assessment
  • Maternal Serum Screen, Alpha Fetoprotein (AFP) for Neural Tube Defect
  • Salicylate, Serum
  • Acanthamoeba and Naegleria Culture and Stains, Corneal Scraping
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  • /Hereditary Hemorrhagic Telangiectasia, ENG 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

Hereditary Hemorrhagic Telangiectasia, ENG Gene Mutation Analysis
Medical Test

Diseases (1)
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