We invite medical workers and professional associations to get involved and help colleagues with advice or find answers that will help patients.
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We invite patients, members of their families and associations to get involved, share their experiences, ask questions.
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We invite companies, individuals, the entire public to help us know that those with rare diseases are not alone.
Read more +The Rare Diseases Database is a unique regional project aimed at shortening the time to diagnosis and providing broad support to patients suffering from rare diseases.
The database is periodically updated and with your suggestions, information and knowledge you can contribute to the improvement of the portal and its content in the relevant segments.
The mission of the Rare Diseases Database is to help doctors and patients, but also to raise awareness among the general public about rare diseases.
Read more about the latest articles and news
| Ana Pataki
U četvrtak 15. aprila 2021. godine, sa početkom u 10 časova, na portalu Baza retkih bolesti organizujemo kontinuiranu medicinsku edukaciju, namenjenu lekarima: „Dijagnostika i lečenje retkih bolesti“....
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| Ana Pataki
Udruženje SMA Srbija organizuje regionalnu konferenciju o spinalnoj mišićnoj atrofiji “Za obolele od SMA i njihovo bolje sutra, 2021”!...
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| Ana Pataki
Najveća korist – razmjena informacija, pronalaženje odgovora na pitanja koja muče pacijente i članove njihovih porodica, ali I ljekare oko postavljanja dijagnoze i terapije....
Read more +Companies and institutions that helped the Rare Diseases Database
