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GTR Home > Laboratories > Collagen Diagnostic Laboratory

Collagen Diagnostic Laboratory

GTR Lab ID: 1058, Last updated:2024-03-28
Annual Review past due read more

Personnel

  • Director: Peter Byers, MD, Lab Director
    Phone: 206-543-4206
    Fax: 206-616-1899
    Email: pbyers@u.washington.edu
  • Director: Ulrike Schwarze, MD, Lab Director
  • Dru Leistritz, MS, Certified Genetic counselor, CGC, Genetic Counselor
    Phone: 206-543-5464
    Fax: 206-616-1899
    Email: dru2@u.washington.edu

Conditions and tests

  • Alport syndrome1 test
  • Aortic aneurysm, familial thoracic 41 test
  • Aortic aneurysm, familial thoracic 61 test
  • Aortic aneurysm, familial thoracic 71 test
  • Aortic aneurysm, familial thoracic 81 test
  • Aortic aneurysm, familial thoracic 91 test
  • Aortic aneurysm, familial thoracic, SMAD3 related1 test
  • Arterial tortuosity syndrome1 test
  • Autosomal dominant Alport syndrome1 test
  • Autosomal recessive Alport syndrome1 test
  • Benign familial hematuria1 test
  • Bone fragility with contractures, arterial rupture, and deafness1 test
  • Bone mineral density quantitative trait locus 181 test
  • Bruck syndrome 11 test
  • Bruck syndrome 21 test
  • Classic homocystinuria1 test
  • Cole-Carpenter syndrome 11 test
  • Cole-Carpenter syndrome 21 test
  • Collagen IV-related nephropathies1 test
  • Congenital contractural arachnodactyly1 test
  • Ehlers-Danlos syndrome2 tests
  • Ehlers-Danlos syndrome progeroid type1 test
  • Ehlers-Danlos syndrome type 7A2 tests
  • Ehlers-Danlos syndrome type 7B2 tests
  • Ehlers-Danlos syndrome, arthrochalasia type1 test
  • Ehlers-Danlos syndrome, classic type2 tests
  • Ehlers-Danlos syndrome, kyphoscoliotic type 11 test
  • Ehlers-Danlos syndrome, kyphoscoliotic type, 22 tests
  • Ehlers-Danlos syndrome, musculocontractural type1 test
  • Ehlers-Danlos syndrome, periodontal type 11 test
  • Ehlers-Danlos syndrome, spondylocheirodysplastic type1 test
  • Ehlers-Danlos syndrome, type 43 tests
  • Familial thoracic aortic aneurysm and aortic dissection2 tests
  • Geroderma osteodysplastica1 test
  • Hyperphosphatasemia with bone disease1 test
  • Hypophosphatasia2 tests
  • Infantile cortical hyperostosis1 test
  • Juvenile polyposis/hereditary hemorrhagic telangiectasia syndrome1 test
  • Larsen-like syndrome, B3GAT3 type1 test
  • Loeys-Dietz syndrome2 tests
  • Marfan syndrome3 tests
  • Marfan Syndrome/Loeys-Dietz Syndrome/Familial Thoracic Aortic Aneurysms and Dissections2 tests
  • Olmsted syndrome, X-linked1 test
  • Osteogenesis imperfecta2 tests
  • Osteogenesis imperfecta type 101 test
  • Osteogenesis imperfecta type 111 test
  • Osteogenesis imperfecta type 121 test
  • Osteogenesis imperfecta type 131 test
  • Osteogenesis imperfecta type 141 test
  • Osteogenesis imperfecta type 151 test
  • Osteogenesis imperfecta type 171 test
  • Osteogenesis imperfecta type 51 test
  • Osteogenesis imperfecta type 71 test
  • Osteogenesis imperfecta type 81 test
  • Osteogenesis imperfecta type 91 test
  • Osteogenesis imperfecta type I1 test
  • Osteogenesis imperfecta with normal sclerae, dominant form1 test
  • Osteoporosis with pseudoglioma1 test
  • Short stature-optic atrophy-Pelger-HuC+t anomaly syndrome1 test
  • Shprintzen-Goldberg syndrome1 test
  • Spondylo-ocular syndrome1 test
  • Sulfate transporter-related osteochondrodysplasia1 test
  • X-linked Alport syndrome2 tests

List of services

  • Clinical Testing/Confirmation of Mutations Identified Previously
  • Confirmation of research findings
  • Carrier testing
  • Genetic counseling

List of certifications/licenses

Certifications

  • CLIAHelp, Number: 50D2093534, Expiration date: 2025-06-05
  • CAP, Number: 9041681, Expiration date: 2023-09-30

Licenses

  • MD - Maryland Department of Health and Mental Hygiene DHMH, Number: 2464, Effective date: 2018-07-01 Non-expiring
  • PA - Pennsylvania Department of Health PADOH, Number: 33890, Expiration date: 2022-08-15

Participation in external programs

Standardization programs

  • 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.