The Ehlers-Danlos syndromes (EDS) are a group of 13 heritable connective tissue disorders. The genetic variants that cause EDS are many and varied in their nature.
To better understand and keep track of these variants, an Ehlers-Danlos Syndrome Variant Database was created. This resource gathers information on genetic variants linked to EDS, allowing healthcare professionals and researchers to identify patterns and enhance medical care.
The Leiden Open Variation Database (LOVD) is an online platform where scientists and healthcare professionals store and share detailed information about genetic variations in human DNA. Researchers, geneticists, and doctors use LOVD to access and contribute data on genetic mutations and variations, helping to link specific DNA changes to various diseases. This shared data aids in diagnosing genetic conditions and developing personalized treatments based on an individual’s genetic makeup. The database includes detailed information about each genetic variant, including its effects on health and related clinical symptoms.