• Hyperthyroidism, primary
  • Muscular Dystrophies Gene Mutation Panel, NGS
  • Ethyl Glucuronide Confirmation, Urine
  • Complement Component C4
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  • Isocitrate Dehydrogenase 2 (IDH2) Mutation Analysis
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  • /HLA-B51 Genotyping for Behçet’s Disease
  • 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

HLA-B51 Genotyping for Behçet’s Disease
Medical Test

Overview
Access to HLA-B51 Genotyping for Behçet’s Disease is restricted.