You are using an outdated browser. Please upgrade your browser to improve your experience.

Ehlers-Danlos syndrome, hypermobility type

Disease Summary
Associated Targets (2)
Tbio

2


GARD Rare
Mondo Description Ehlers-Danlos syndrome, hypermobility type (HT-EDS) is the most frequent form of EDS, a group of hereditary connective tissue diseases, and is characterized by joint hyperlaxity, mild skin hyperextensibility, tissue fragility and extra-musculoskeletal manifestations.
Mondo Term and Equivalent IDs
MONDO:0007523:  Ehlers-Danlos syndrome, hypermobility type
GARD:0002081: 
MESH:C536196: 
NCIT:C125698: 
Orphanet:285: 
SCTID:30652003: 
UMLS:C0268337: