FinDis

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