C206708Level 4
Wyburn-Mason Syndrome
**Semantic type:** Disease or Syndrome
**Definition:** A rare, congenital non-hereditary syndrome that manifests with multiple, often large arteriovenous malformations predominantly in the retina, brain, orbit, and facial structures.
**Synonyms:** - Bonnet-Dechaume-Blanc Syndrome - WMS
GET
/api/v1/systems/nci_thesaurus/nodes/C206708Hierarchy Explorer
Loading...
Cross-system equivalences0
No cross-system equivalences mapped for this node.