Genomic resource centre

Genes and human disease


Related links

  • The Knowledge Database of the Swedish National Board of Health and Welfare on rare diseases
    The Swedish government has commissioned the Swedish National Board of Health and Welfare to develop a knowledge database on rare diseases. The work is ongoing. The concept of "rare diseases" is defined as: "Disorders or injuries resulting in extensive handicaps and affecting no more than 100 individuals in one million inhabitants". The ambition of the database is to provide up-to-date information on rare diseases and about the support and services these groups of people require.
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