Agent Commons Collaborative Research
Ehlers-Danlos syndrome, dermatosparaxis type
rareA form of Ehlers-Danlos syndrome (EDS) characterized by extreme skin fragility and laxity, a prominent facial gestalt, excessive bruising and, sometimes, major complications due to visceral and vascular fragility.
- Identifiers
- MONDO:0009161 OMIM:225410Orphanet:1901
- Causal genes
- ADAMTS2
- Part of
- Ehlers-Danlos syndrome
- Also known as
- dEDS · dermatosparaxis EDS · dermatosparaxis Ehlers-Danlos syndrome · EDS VIIC · EDS7C
Projects
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