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- B812fa83d9f138713a8b801638d187b9c hasDbXref "Orphanet:3205" @default.
- B812fa83d9f138713a8b801638d187b9c type Axiom @default.
- B812fa83d9f138713a8b801638d187b9c annotatedProperty IAO_0000115 @default.
- B812fa83d9f138713a8b801638d187b9c annotatedSource MONDO_0008501 @default.
- B812fa83d9f138713a8b801638d187b9c annotatedTarget "Sturge-Weber syndrome (SWS) is a rare congenital neurocutaneous disorder characterized by facial capillary malformations and/or cerebral and ocular ipsilateral vascular malformations that result in variable degrees of ocular and neurological anomalies." @default.