A rare disease, also referred to as an ‘orphan’ disease, is considered as a disease which affects less than 5 per 10,000 of the European population. Most rare diseases are genetic, and commonly present in childhood. The database is dedicated to providing disease descriptions, genetic testing and genetic mutations.

• Subject category: Child health
• Database Type: Health Databases
• Access Resource: https://www.eurordis.org/content/rare-disease-databases

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