• Trisomy 21 (Down syndrome)
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  • Solute carrier family 6 member 2 (SLC6A2)
  • Microsomal epoxide hydrolase 1 (EPHX1) Gene Variation
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  • All
  • Diseases
  • Overview
  • Clinical Utility
  • Interpretation
  • Reference Ranges
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  • Specimen Collection
  • Additional Testing
  • Turnaround Time
  • CPT
  • LOINC
  • ICD10
  • Additional ICD10
  • References

Phenytoin, Urine
Medical Test

Diseases (1)
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