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GTR Home > Laboratories > Department of Clinical Genetics

Department of Clinical Genetics

GTR Lab ID: 241586, Last updated:2023-01-27
Annual Review past due read more

Personnel

  • Director: Klaus Brusgaard, PhD, MSc, Lab Director
    Phone: +45 65412874
    Fax: +45 65411811
    Email: Klaus.brusgaard@rsyd.dk
  • Director: Lotte Krogh, Lab Director
    Phone: +45 6541-2878
    Fax: +45 6541-1911
    Email: lotte.krogh@rsyd.dk

Conditions and tests

  • Acute intermittent porphyria1 test
  • Cutaneous porphyria1 test
  • Exercise-induced hyperinsulinism1 test
  • Familial porphyria cutanea tarda1 test
  • Familial X-linked hypophosphatemic vitamin D refractory rickets1 test
  • Hepatoerythropoietic porphyria1 test
  • Hereditary coproporphyria1 test
  • Hereditary pancreatitis3 tests
  • Hyperinsulinemia1 test
  • Hyperinsulinemic hypoglycemia, familial, 13 tests
  • Hyperinsulinemic hypoglycemia, familial, 21 test
  • Hyperinsulinemic hypoglycemia, familial, 41 test
  • Hyperinsulinism due to glucokinase deficiency1 test
  • Hyperinsulinism due to INSR deficiency1 test
  • Hyperinsulinism-hyperammonemia syndrome1 test
  • Insulin-dependent diabetes mellitus secretory diarrhea syndrome1 test
  • Juvenile polyposis/hereditary hemorrhagic telangiectasia syndrome1 test
  • Leprechaunism syndrome1 test
  • Maturity onset diabetes mellitus in young1 test
  • Maturity-onset diabetes of the young type 11 test
  • Maturity-onset diabetes of the young type 101 test
  • Maturity-onset diabetes of the young type 111 test
  • Maturity-onset diabetes of the young type 21 test
  • Maturity-onset diabetes of the young type 31 test
  • Maturity-onset diabetes of the young type 41 test
  • Maturity-onset diabetes of the young type 61 test
  • Maturity-onset diabetes of the young type 71 test
  • Maturity-onset diabetes of the young type 81 test
  • Neonatal diabetes mellitus1 test
  • Neonatal diabetes mellitus with congenital hypothyroidism1 test
  • Permanent neonatal diabetes mellitus1 test
  • Porphyria cutanea tarda1 test
  • Protoporphyria, erythropoietic, 11 test
  • Telangiectasia, hereditary hemorrhagic, type 21 test
  • Variegate porphyria1 test
  • Wolcott-Rallison dysplasia1 test
  • X-linked erythropoietic protoporphyria1 test

List of services

  • Clinical Testing/Confirmation of Mutations Identified Previously

List of certifications/licenses

Certifications

  • ISO15189, Number: 1024, Expiration date: 2023-02-28

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.