se-atlas – the health service information platform for people with rare diseases

The jorunal Bundesgesundheitsblatt Gesundheitsforschung Gesundheitsschutz has published an article about se-atlas. se-atlas – the health service information platform for rare diseases – is part of the German National Action Plan for People with Rare Diseases and is funded by the German Federal Ministry of Health. The objective of se-atlas as a web-based platform is to illustrate those medical care institutions that are linked to rare diseases, in a transparent and user-friendly way. The full-text article you can find here.