• Familial Hypercholesterolemia and Related Diseases Multi-Gene Panel, NGS
  • Carnitine Palmitoyltransferase II Deficiency, Gene Mutation Analysis
  • Adenovirus DNA, Real-time PCR, Qualitative
  • Iron, Serum
  • Herpes Simplex Virus (HSV) 1 and 2, Immunoblot
  • Poly A Binding Protein Nuclear 1Gene (PABPN1) Mutation Analysis
  • Telomere Defects Gene Mutation Panel, NGS
  • Paroxysmal nocturnal hemoglobinuria
  • CaM Kinase II (CaMKII, Calcium-dependent Calmodulin Protein Kinase II) Activation
  • Topiramate, Urine
  • LDS
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  • /Complement Component CH50
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  • All
  • Diseases
  • Overview
  • Clinical Utility
  • Interpretation
  • Reference Ranges
  • Methodology
  • Specimen Collection
  • Additional Testing
  • Turnaround Time
  • CPT
  • ICD10
  • Additional ICD10
  • References

Complement Component CH50
Medical Test

Specimen Collection
Access to Complement Component CH50 is restricted.