Is orphanet Journal of rare diseases peer reviewed?
Aims and scope Orphanet Journal of Rare Diseases is an open access, peer-reviewed journal that encompasses all aspects of rare diseases and orphan drugs. The journal publishes high-quality reviews on specific rare diseases.
What is the orphanet database?
Orphanet is a unique resource, gathering and improving knowledge on rare diseases so as to improve the diagnosis, care and treatment of patients with rare diseases. Orphanet aims to provide high-quality information on rare diseases, and ensure equal access to knowledge for all stakeholders.
How do you cite orphanet?
When citing an Orphanet disease profile, the following format is appropriate : Author(s). Rare Disease name. Orphanet encyclopedia, Month, Year, Corresponding URL.
How is rare disease defined?
What is a rare disease? The Orphan Drug Act defines a rare disease as a disease or condition that affects less than 200,000 people in the United States. Back to top. What is the Orphan Drug Act? The Orphan Drug Act is a law passed by Congress in 1983 that incentivizes the development of drugs to treat rare diseases.
How many types of rare diseases are there?
How many rare diseases are there? There are more than 7,000 rare diseases, according to the National Institutes of Health (NIH).
What is the meaning of Orphanet?
Orphanet is an online database with the aspiration of gathering, providing and improving knowledge on rare diseases and to improve the diagnosis, care and treatment of patients with rare diseases.
How are rare diseases diagnosed?
In general, final diagnosis for most rare diseases is performed using a genetic test that tends to be focused on a small set of diseases.
How common is a rare disease?
How many people have rare diseases? According to the National Institutes of Health (NIH), there are approximately 7,000 rare diseases affecting between 25 and 30 million Americans. This equates to 1 in 10 Americans, or one on every elevator and four on every bus.
How many rare diseases are there orphanet?
It includes an encyclopedia of rare diseases covering more than 1,300 diseases which is expert-authored and peer-reviewed, and a directory of services in Europe, including information on specialized clinics, clinical laboratories, ongoing research projects, clinical trials, registries, and support groups.