FinDis is a centralized resource for cross-referenced information on disease mutations enriched in the Finnish population.

FinDis provides up-to-date information on the 35 monogenic diseases belonging to the Finnish disease heritage, browsable by Diseases or Genes.

For each disease, this resource provides:

  • Prevalence or incidence and a short description of clinical symptoms
  • Genetic locus and a molecular description for identified mutations
  • Character and consequences of all known mutations, Finnish and foreign, described at the DNA and polypeptide levels
  • Disease allele frequencies typically reported for Finnish mutations
  • A comprehensive list of publications

FinDis has received funding from the Academy of Finland, Center of Excellence in Disease Genetics
and the European Community's Seventh Framework Programme (FP7/2007-2013) under grant agreement number 200754 - the GEN2PHEN project.