GTR Home > Laboratories > Department of Clinical Genetics

Department of Clinical Genetics

GTR Lab ID: 241586
Last updated: 2013-10-30

General information

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Conditions and tests

  • ACVRL1-Related Hereditary Hemorrhagic Telangiectasia1 test
  • AIP-Related Familial Isolated Pituitary Adenomas1 test
  • Acute Intermittent Porphyria1 test
  • COL4A5-Related Nephropathy1 test
  • ENG-Related Hereditary Hemorrhagic Telangiectasia1 test
  • Erythropoietic Protoporphyria, Autosomal Recessive1 test
  • Familial Hyperinsulinism1 test
  • GLUD1-Related Hyperinsulinism1 test
  • Hereditary Coproporphyria1 test
  • KCNJ11-Related Hyperinsulinism1 test
  • Maturity-Onset Diabetes of the Young Type 11 test
  • Maturity-Onset Diabetes of the Young Type 21 test
  • Maturity-Onset Diabetes of the Young Type 31 test
  • PRSS1-Related Hereditary Pancreatitis1 test
  • Persistent hyperinsulinemic hypoglycemia of infancy1 test
  • Renal Cysts and Diabetes Syndrome1 test
  • SMAD4-Related Hereditary Hemorrhagic Telangiectasia1 test
  • UROD-Related Porphyrias1 test
  • Variegate Porphyria1 test
  • X-Linked Hypophosphatemia1 test

List of services

  • Clinical Testing/Confirmation of Mutations Identified Previously

List of certifications/licenses


  • DDKM, Number: UNSP, Expiration date: 2014-05-01

Participation in external programs

Standardization programs

  • Locus-specific Databases
  • Mutation-specific Databases

Data exchange Programs

  • Locus-specific Databases
  • Mutation-specific Databases

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.

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