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GTR Home > Laboratories > Connective Tissue Laboratory

Connective Tissue Laboratory

  • Connective Tissue Laboratory
  • Ghent University Hospital (UZ Gent)
  • Department: Center for Medical Genetics Ghent
  • Corneel Heymanslaan 10
  • Ghent, Oost-Vlaanderen, Belgium 9000
  • Phone: +32 93323603
    Fax: +32 93326549
    Email: connective_tissue@cmgg.be
  • Website: https://www.cmgg.be/

GTR Lab ID: 320197, Last updated:2024-01-16


Conditions and tests

  • Achondrogenesis type II2 tests
  • ALDH18A1-related de Barsy syndrome11 tests
  • Aneurysm-osteoarthritis syndrome11 tests
  • Aortic aneurysm, familial thoracic 411 tests
  • Aortic aneurysm, familial thoracic 611 tests
  • Aortic aneurysm, familial thoracic 710 tests
  • Aortic aneurysm, familial thoracic 810 tests
  • Aortic valve disease 110 tests
  • Arrhythmogenic right ventricular dysplasia 111 tests
  • Arterial calcification, generalized, of infancy, 14 tests
  • Arterial calcification, generalized, of infancy, 24 tests
  • Arterial tortuosity syndrome10 tests
  • Autosomal recessive cutis laxa type 2B11 tests
  • Autosomal recessive inherited pseudoxanthoma elasticum4 tests
  • Avascular necrosis of femoral head, primary, 12 tests
  • Bethlem myopathy 1A5 tests
  • Body skin hyperlaxity due to vitamin K-dependent coagulation factor deficiency4 tests
  • Brain small vessel disease 1 with or without ocular anomalies3 tests
  • Brittle cornea syndrome 13 tests
  • Brittle cornea syndrome 23 tests
  • Cardiac valvular dysplasia, X-linked9 tests
  • Congenital contractural arachnodactyly10 tests
  • Cutis laxa with osteodystrophy11 tests
  • Cutis laxa with severe pulmonary, gastrointestinal and urinary anomalies11 tests
  • Cutis laxa, autosomal dominant 119 tests
  • Cutis laxa, autosomal dominant 211 tests
  • Cutis laxa, autosomal recessive1 test
  • Cutis laxa, autosomal recessive, type 1A11 tests
  • Cutis laxa, autosomal recessive, type 1B19 tests
  • Cutis laxa, X-linked11 tests
  • Ectopia lentis 1, isolated, autosomal dominant4 tests
  • Ectopia lentis 2, isolated, autosomal recessive4 tests
  • Ectopia lentis et pupillae4 tests
  • Ehlers-Danlos syndrome progeroid type11 tests
  • Ehlers-Danlos syndrome, classic type3 tests
  • Ehlers-Danlos syndrome, classic type, 13 tests
  • Ehlers-Danlos syndrome, dermatosparaxis type11 tests
  • Ehlers-Danlos syndrome, kyphoscoliotic and deafness type11 tests
  • Ehlers-Danlos syndrome, kyphoscoliotic type 111 tests
  • Ehlers-Danlos syndrome, musculocontractural type11 tests
  • Ehlers-Danlos syndrome, musculocontractural type 211 tests
  • Ehlers-Danlos syndrome, spondylocheirodysplastic type11 tests
  • Ehlers-Danlos syndrome, spondylodysplastic type, 211 tests
  • Ehlers-Danlos syndrome, type 412 tests
  • Geroderma osteodysplastica11 tests
  • Kniest dysplasia2 tests
  • Larsen-like syndrome, B3GAT3 type11 tests
  • Legg-Calve-Perthes disease2 tests
  • Loeys-Dietz syndrome 111 tests
  • Loeys-Dietz syndrome 211 tests
  • Loeys-Dietz syndrome 411 tests
  • Marfan syndrome11 tests
  • MASS syndrome11 tests
  • Menkes kinky-hair syndrome11 tests
  • Microspherophakia4 tests
  • Moyamoya disease 511 tests
  • Multiple epiphyseal dysplasia, Beighton type2 tests
  • Multisystemic smooth muscle dysfunction syndrome11 tests
  • Namaqualand hip dysplasia2 tests
  • Osteogenesis imperfecta15 tests
  • Osteogenesis imperfecta type I3 tests
  • Osteogenesis imperfecta type III3 tests
  • Osteogenesis imperfecta with normal sclerae, dominant form3 tests
  • Osteogenesis imperfecta, perinatal lethal3 tests
  • Otospondylomegaepiphyseal dysplasia, autosomal dominant4 tests
  • Otospondylomegaepiphyseal dysplasia, autosomal recessive2 tests
  • Platyspondylic dysplasia, Torrance type2 tests
  • Porencephaly 23 tests
  • Pseudoxanthoma elasticum, forme fruste4 tests
  • PYCR1-related de Barsy syndrome11 tests
  • RIN2 syndrome2 tests
  • Shprintzen-Goldberg syndrome11 tests
  • Spondyloepimetaphyseal dysplasia with joint laxity, type 1, with or without fractures11 tests
  • Spondyloepiphyseal dysplasia congenita2 tests
  • Spondyloepiphyseal dysplasia with metatarsal shortening2 tests
  • Spondylometaphyseal dysplasia2 tests
  • Spondyloperipheral dysplasia2 tests
  • Stickler syndrome1 test
  • Stickler syndrome type 14 tests
  • Stickler syndrome type 24 tests
  • Stickler syndrome, type I, nonsyndromic ocular4 tests
  • Stiff skin syndrome11 tests
  • Supravalvar aortic stenosis19 tests
  • Type II Collagenopathies1 test
  • Ullrich congenital muscular dystrophy 1A5 tests
  • Vitamin K-dependent clotting factors, combined deficiency of, type 14 tests
  • Weill-Marchesani syndrome 110 tests
  • Weill-Marchesani syndrome 2, dominant11 tests
  • Wrinkly skin syndrome11 tests

List of services

  • This lab has no services.

List of certifications/licenses


  • ISO15189, Number: 351-MED, Expiration date: 2021-09-10

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