• Vascular Endothelial Growth Factor (VEGF)
  • Integrin Subunit Beta 3 (ITGB3) Gene Mutation Analysis
  • Culture, Synovial Fluid
  • 17-Hydroxypregnenolone, Serum
  • Hematocrit/Microhematocrit
  • Parvovirus B19 Antibody, IgG
  • Pseudocholinesterase, Total, Serum
  • Obstetric Panel
  • Drug Testing, Definitive (Drug Identification by Confirmatory Method), Multi-drug Panel, Urine
  • Hereditary Angioedema Diagnostic Panel
  • LDS
  • Sign up
  • Log in
  • LDS
  • /Medical Tests
  • /von Willebrand Disease 2N (Subtype Normandy), Genotyping
  • 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

von Willebrand Disease 2N (Subtype Normandy), Genotyping
Medical Test

Additional ICD10
Access to von Willebrand Disease 2N (Subtype Normandy), Genotyping is restricted.
Loading...