Ehlers-Danlos syndrome
MONDO:0020066Also known as: Danlos Disease, Ehlers, Danlos disease, Disease, Ehlers Danlos, Disease, Ehlers-Danlos, Dystrophia mesodermalis congenita
- MONDO:
- MONDO:0020066
- Orphanet:
- 98249 ↗
Rare disease36 associated genes
Description
The Ehlers–Danlos syndromes (EDS) are a clinically and genetically heterogeneous group of heritable connective tissue disorders (HCTDs) characterized by joint hypermobility, skin hyperextensibility, and tissue fragility.
Associated genes
+26 more genes — install the extension to see the full list inline on any page.