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FAH Remaining Exons Sequencing

FORMS AND DOCUMENTS

TEST DETAILS

Genes:
FAH
Disorders:
Clinical Utility:
  • Confirmation of biochemical diagnosis
  • Carrier testing
  • Prenatal diagnosis in at risk pregnancies
Lab Method:
Capillary Sequencing

ORDERING

Test Code:
3663
Turnaround Time:
4-5 weeks
Preferred Specimen:
2-5 mL Blood - Lavender Top Tube

BILLING

CPT Codes:
81406x1
New York Approved:
No
ABN Required:
Yes
Billing Information:
View Billing Policy
ICD Codes:
  • 796.6: Abnormal findings on neonatal screening
  • 270.2: Other disturbances of aromatic amino-acid metabolism, Albinism, Alkaptonuria, Alkaptonuric ochronosis, Disturbances of metabolism of tyrosine and tryptophan, Homogentisic acid defects, Hydroxykynureninuria Hypertyrosinemia, Indicanuria, Kynureninase defects, Oasthouse urine disease, Ochronosis, Tyrosinosis, Tyrosinuria, Waardenburg syndrome
* For price inquiries please email zebras@genedx.com

REFERENCES

  1. Rootwelt et al., (1994) Am J Hum Genet 55 :1122-1127
  2. Bergman et al., (1998) Hum Mutat 12 :19-26
  3. Grompe et al., (1994) N Engl J Med 11(6):353-7
  4. St-Louis, M. and Tanguay R.M. (1997) Hum Mutat 9 :291- 299
  5. Arranz et al., (2002) Hum Mutat 20:180-188

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