Genetic Testing Company | The DNA Diagnostic Experts | GeneDx

In observance of the holidays, GeneDx will be closed for business on Thursday, December 25, 2014 and on Thursday, January 1, 2015. We will be unable to receive and process specimens. FedEx and UPS will also not be in operation. Except for the aforementioned dates, GeneDx will operate on our normal schedule (Monday-Saturday), including December 24th and December 31st.  If you have any questions or inquiries, please call us at 301-519-2100 or email us at zebras@genedx.com.

NCF2 Gene Sequencing

FORMS AND DOCUMENTS

TEST DETAILS

Genes:
NCF2
Disorders:
Clinical Utility:
  • Confirmation of clinical or laboratory diagnosis.
  • Identification of the involved gene
  • Carrier testing or rapid diagnosis in relatives
  • Prenatal diagnosis
Lab Method:
Capillary Sequencing

ORDERING

Test Code:
1437
Turnaround Time:
5-6 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. Heyworth PG, et al, 2001, Hematologically Important Mutations: X-linked chronic granulomatous disease (second update), Blood Cells Molecules and Diseases 27:16
  2. Yu G et al, 2008, Focus on FOCIS: The continuing diagnostic challenge of autosomal recessive chronic granulomatous disease

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