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GTR Home > Laboratories > Genetics Laboratory, Peroxisomal Disorders Section

Genetics Laboratory, Peroxisomal Disorders Section

GTR Lab ID: 1003, Last updated:2023-06-16
Annual Review past due read more

Personnel

Conditions and tests

  • Acyl-CoA oxidase deficiency2 tests
  • Adrenoleukodystrophy3 tests
  • Bifunctional peroxisomal enzyme deficiency2 tests
  • Peroxisome biogenesis disorder6 tests
  • Phytanic acid storage disease1 test
  • Pyridoxine-dependent epilepsy1 test
  • Rhizomelic chondrodysplasia punctata type 13 tests
  • Rhizomelic chondrodysplasia punctata type 22 tests
  • Rhizomelic chondrodysplasia punctata type 32 tests

List of services

  • Clinical Testing/Confirmation of Mutations Identified Previously

List of certifications/licenses

Certifications

  • CLIAHelp, Number: 21D0649789, Expiration date: 2023-11-30
  • CAP, Number: 1353022, Expiration date: 2025-06-30

Licenses

  • CA - California Department of Public Health CDPH, Number: CDS00800866, Expiration date: 2024-05-16
  • MD - Maryland Department of Health and Mental Hygiene DHMH, Number: 802, Effective date: 2018-07-01 Non-expiring
  • PA - Pennsylvania Department of Health PADOH, Number: 033873, Expiration date: 2023-08-15

IMPORTANT NOTE: NIH does not independently verify information submitted to the GTR; it relies on submitters to provide information that is accurate and not misleading. NIH makes no endorsements of tests or laboratories listed in the GTR. GTR is not a substitute for medical advice. Patients and consumers with specific questions about a genetic test should contact a health care provider or a genetics professional.