• Adenosine Deaminase, CSF
  • POEMS syndrome
  • Respiratory alkalosis
  • Sickle Cell Screen
  • Quinidine, Urine
  • Medium-Chain Acyl-CoA Dehydrogenase (MCAD) Mutation Analysis
  • Secobarbital, Urine
  • Beta-2 Glycoprotein 1 Antibody Panel (IgA, IgG, IgM)
  • Multiple Sulfatase Deficiency, Gene Mutation Analysis
  • ABO Group and Rh Typing
  • LDS
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  • /HLA-B51 Genotyping for Behçet’s Disease
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  • 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

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