Sturge-Weber Syndrome Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
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)
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2 genes/proteins associated with the disease Sturge-Weber Syndrome from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
RASA1 RAS p21 protein activator (GTPase activating protein) 1 2.88009
GNAQ guanine nucleotide binding protein (G protein), q polypeptide 2.88009