• Carbohydrate Deficient Transferrin for Congenital Disorders of Glycosylation, Serum
  • Phospholipid (Cardiolipin) Antibody Panel, IgA, IgG, IgM
  • Biopsy, Salivary Gland
  • Hepatitis C Virus (HCV) NS3/4A Protease Inhibitor Resistance, GenoSure
  • Calcium, 24 Hour, Urine
  • Aspergillus (Galactomannan) Antigen, Serum
  • MLYCD Gene Mutation Analysis, Tissue
  • Angiotensin Converting Enzyme (ACE), CSF
  • Protein S, Functional
  • AIRE gene mutation
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  • /Hereditary Hemorrhagic Telangiectasia, ENG Gene Mutation Analysis
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  • Methodology
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  • CPT
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  • Additional ICD10
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  • 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

Additional ICD10
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