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. The disease is Sturge-Weber syndrome (MONDO_0008501, a Monarch Disease Ontology id). Also known as: SWS, Sturge Weber Syndrome, Sturge Weber syndrome, Sturge-Weber disease, Sturge-Weber syndrome, somatic, mosaic, Sturge-Weber-Dimitri syndrome, Sturge-Weber-Krabbe angiomatosis, Sturge-Weber-Krabbe syndrome.