Genetic Testing Company | The DNA Diagnostic Experts | GeneDx

CGD Tier 1

FORMS AND DOCUMENTS

TEST DETAILS

Genes:
CYBB, NCF1 (Exon 2)
Disorders:
Clinical Utility:
  • Confirmation of clinical or laboratory diagnosis.
  • Identification of the involved gene and the specific mutation to permit accurate genetic counseling.
  • Carrier testing or rapid diagnosis in relatives
  • Prenatal diagnosis
Lab Method:
Capillary Sequencing

ORDERING

Test Code:
1431
Turnaround Time:
6-7 weeks
Preferred Specimen:
2-5 mL Blood - Lavender Top Tube

BILLING

CPT Codes:
81479x1
New York Approved:
No
ABN Required:
Yes
Billing Information:
View Billing Policy
ICD Codes:
  • 288.1: Functional disorders of polymorphonuclear neutrophils, Chronic (childhood) granulomatous disease, Congenital dysphagocytosis, Job's syndrome, Lipochrome histiocytosis (familial), Progressive septic granulomatosis
* For price inquiries please email zebras@genedx.com

REFERENCES

  1. Yu G et al, 2008, Focus on FOCIS: The continuing diagnostic challenge of autosomal recessive chronic granulomatous disease.
  2. Heyworth PG, et al, 2001, Hematologically Important Mutations: X-linked chronic granulomatous disease (second update), Blood Cells Molecules and Diseases 27:16.

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