|Dataset||CTD Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||A rare congenital syndrome characterized by large cutaneous hemangiomata with hypertrophy of the related bones and soft tissues. (Human Disease Ontology, DOID_2926)|
|Downloads & Tools|
2 genes/proteins associated with the disease Klippel-Trenaunay-Weber Syndrome from the curated CTD Gene-Disease Associations dataset.