|Dataset||CTD Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||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. (Orphanet Rare Disease Ontology, Orphanet_3205)|
|Downloads & Tools|
2 genes/proteins associated with the disease Sturge-Weber Syndrome from the curated CTD Gene-Disease Associations dataset.