• Oncotype DX, Prostate Cancer
  • Anaplasma phagocytophilum Molecular Detection, PCR
  • Acute Myeloid Leukemia (AML), FISH, Bone Marrow
  • Huntington Disease Mutation Analysis
  • Gene Expression Profile for Cutaneous Melanoma, DermTech (DecisionDx®-SCC), Pigmented Lesion Assay (PLA), myPath® Melanoma
  • Bilirubin Total, Serum
  • von Willebrand Disease 2N (Subtype Normandy), Genotyping
  • Coccidioides Antibody, IgM
  • Chromogranin A
  • Sickle Cell Screen
  • LDS
  • Sign up
  • Log in
  • LDS
  • /Medical Tests
  • /X-Linked Adrenoleukodystrophy (ABCD1) Gene Mutation Analysis, Blood
  • 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

X-Linked Adrenoleukodystrophy (ABCD1) Gene Mutation Analysis, Blood
Medical Test

CPT
Access to X-Linked Adrenoleukodystrophy (ABCD1) Gene Mutation Analysis, Blood is restricted.