There is no disease so rare
that it does not deserve attention

• • AUSTRIA
  • TIROL
  • INNSBRUCK
  • Austrian Country Node of the Human Variome Project (HVP)
  • Medizinische Universität Innsbruck
  • Sektion Humangenetik
  • More details
• • DENMARK
  • Sjælland
  • COPENHAGEN
  • Mendelian cytogenetics network online database
  • The Panum Institute-University of Copenhagen
  • Department of Cellular and Molecular Medicine
  • More details
• • ESTONIA
  • Tartu
  • TARTU
  • Biobank of the Estonian genome center
  • Tartu University Hospital
  • Centre of Genetics - United laboratories
  • More details
• • FINLAND
  • Finland
  • HELSINKI
  • The Finnish Register of Visual Impairment
  • Finnish Federation of the Visually Impaired
  • More details
• • FRANCE
  • ILE-DE-FRANCE
  • PARIS
  • Cohort of patients with hereditary dystrophies of retina
  • CHU Paris Est - Hôpital Saint-Antoine
  • Centre de Recherches Institut de la Vision
  • More details
• • GERMANY
  • Baden-Württemberg
  • TÜBINGEN
  • RetDis Database: blood or DNA samples of patients and families with inherited eye diseases
  • Universitätsklinik Tübingen
  • Molekulargenetisches Labor
  • More details
• • GERMANY
  • Baden-Württemberg
  • TÜBINGEN
  • RetDis Database: clinical descriptions of patients and families with inherited eye diseases
  • Universitätsklinik Tübingen
  • Molekulargenetisches Labor
  • More details
• • MOROCCO
  • Rabat
  • RABAT
  • MoHuMuDa : Moroccan Human Mutation Database
  • Institut National d'Hygiène
  • Département de génétique médicale
  • More details
• • SPAIN
  • Madrid
  • MADRID
  • Spanish patient registry of hereditary retinal dystrophy
  • Fundación Jiménez Díaz
  • Servicio de Genética Médica
  • More details
• • UNITED KINGDOM
  • Greater Manchester
  • MANCHESTER
  • DMuDB: Diagnostic Mutation Database
  • St Mary's Hospital
  • National Genetics Reference Laboratory - Manchester
  • More details