• Severe Combined Immunodeficiency Gene Panel, NGS
  • Darkfield Microscopy
  • ATP-binding cassette transporter A1 (ABCA1) Genotyping
  • Connective Tissue Disease Profile (Extractable Nuclear Antigen Antibody Panel)
  • Oxalate, 24 Hour, Urine
  • Galactokinase, Blood
  • Complete Blood Cell Count (CBC) with Differential
  • Eosinophils, Nasal
  • Desipramine, Serum
  • Calcitonin (Thyrocalcitonin)
  • LDS
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  • /Solute Carrier Family 22 (SLC22A5) Gene Mutation Analysis
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  • Interpretation
  • Reference Ranges
  • Methodology
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  • 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

Solute Carrier Family 22 (SLC22A5) Gene Mutation Analysis
Medical Test

LOINC
Access to Solute Carrier Family 22 (SLC22A5) Gene Mutation Analysis is restricted.