• HLA-B27 Genotyping, Ankylosing Spondylitis
  • Erythrocyte Sedimentation Rate (ESR)
  • Microsatellite Instability (MSI), HNPCC/Lynch Syndrome
  • HLA C Genotype
  • Cancer Antigen (CA) 19-9, Peritoneal Fluid
  • ATP-binding cassette transporter A1 (ABCA1) Genotyping
  • Albumin, 24 Hour, Urine
  • Pipecolic Acid, Urine
  • HLA Class II DR, DQ and DP Genotyping (HLA-DRB1, -DRB3/4/5, -DQB1, -DQA1, -DPB1, or -DPA1)
  • Squamous Cell Carcinoma Antigen (SSCA)
  • LDS
  • Sign up
  • Log in
  • LDS
  • /Medical Tests
  • /Hereditary Hemolytic Anemia Gene Mutation Panel, NGS
  • All
  • Diseases
  • Overview
  • Clinical Utility
  • Interpretation
  • Reference Ranges
  • Methodology
  • Specimen Collection
  • Additional Testing
  • Turnaround Time
  • CPT
  • ICD10
  • Additional ICD10
  • References
  • All
  • Diseases
  • Overview
  • Clinical Utility
  • Interpretation
  • Reference Ranges
  • Methodology
  • Specimen Collection
  • Additional Testing
  • Turnaround Time
  • CPT
  • ICD10
  • Additional ICD10
  • References

Hereditary Hemolytic Anemia Gene Mutation Panel, NGS
Medical Test

Methodology
Access to Hereditary Hemolytic Anemia Gene Mutation Panel, NGS is restricted.