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Laboratory of Genetics

GTR Lab ID: 209419, Last updated:2017-06-07


Conditions and tests

  • Alzheimer disease, type 31 test
  • Argininosuccinate lyase deficiency1 test
  • Aspartylglycosaminuria1 test
  • Autosomal recessive polycystic kidney disease1 test
  • Breast-ovarian cancer, familial 11 test
  • Bronchiectasis1 test
  • Cartilage-Hair Hypoplasia-Anauxetic Dysplasia Spectrum Disorders1 test
  • Ceroid lipofuscinosis neuronal 11 test
  • Ceroid lipofuscinosis neuronal 51 test
  • Ceroid lipofuscinosis neuronal 81 test
  • Choroideremia1 test
  • Cohen syndrome1 test
  • Congenital bilateral absence of the vas deferens1 test
  • Congenital secretory diarrhea, chloride type1 test
  • Corneal dystrophy1 test
  • Cystic fibrosis1 test
  • Deafness, autosomal recessive 1A1 test
  • Distal myopathy Markesbery-Griggs type1 test
  • Finnish congenital nephrotic syndrome1 test
  • GRACILE syndrome1 test
  • Hemochromatosis type 11 test
  • Hereditary breast and ovarian cancer syndrome2 tests
  • Huntington's chorea1 test
  • Hydrolethalus syndrome 11 test
  • Juvenile myopathy, encephalopathy, lactic acidosis AND stroke1 test
  • Juvenile neuronal ceroid lipofuscinosis1 test
  • Juvenile retinoschisis1 test
  • Leber's optic atrophy1 test
  • Lethal arthrogryposis with anterior horn cell disease1 test
  • Lethal congenital contracture syndrome 11 test
  • Lynch syndrome II2 tests
  • Meckel syndrome type 61 test
  • Medium-chain acyl-coenzyme A dehydrogenase deficiency1 test
  • Meretoja syndrome1 test
  • Mitochondrial DNA depletion syndrome 7 (hepatocerebral type)1 test
  • Mitochondrial DNA-Associated Leigh Syndrome and NARP1 test
  • Mitochondrial trifunctional protein deficiency1 test
  • Mulibrey nanism syndrome1 test
  • Multiple endocrine neoplasia, type 21 test
  • Muscle eye brain disease1 test
  • MYH-associated polyposis1 test
  • Nephronophthisis 11 test
  • Osteochondrodysplasia1 test
  • Ovarian dysgenesis 11 test
  • Polyglandular autoimmune syndrome, type 11 test
  • Progressive sclerosing poliodystrophy1 test
  • Rett syndrome1 test
  • Salla disease1 test
  • Spondyloarthropathy, susceptibility to1 test
  • Steinert myotonic dystrophy syndrome1 test
  • Thrombophilia1 test
  • Thrombophilia due to activated protein C resistance1 test
  • Unverricht-Lundborg syndrome1 test
  • Usher syndrome, type 3A1 test

List of services

  • This lab has no services.

List of certifications/licenses


  • ISO15189, Number: FINAS 2014/62/60, Expiration date: 2020-10-15

Participation in external programs

Standardization programs

  • Other

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