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TAT Del/Dup

FORMS AND DOCUMENTS

TEST DETAILS

Genes:
TAT
Disorders:
Clinical Utility:
  • Confirmation of biochemical diagnosis
  • Carrier testing
  • Prenatal diagnosis in at risk pregnancies
Lab Method:
Exon Array CGH

ORDERING

Test Code:
906
Turnaround Time:
3-4 weeks
Preferred Specimen:
2-5 mL Blood - Lavender Top Tube

BILLING

CPT Codes:
84311x1, 88271x10, 88291x1
New York Approved:
Yes
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. Natt et al., (1987) Hum Genet 77:352-358.
  2. Charfeddine et al., (2006) Mol Genet Metab 88:184-191.
  3. Maydan et al., (2006) J Inherit Metab Dis 29:620-626.
  4. Huhn et al., (1998) Hum Genet 102:305-313.
  5. Natt et al., (1992) Proc Natl Acad Sci 89:9297-9301.

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