Klippel-Trenaunay-Weber Syndrome Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A rare congenital syndrome characterized by large cutaneous hemangiomata with hypertrophy of the related bones and soft tissues. (Human Disease Ontology, DOID_2926)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:D007715
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2 genes/proteins associated with the disease Klippel-Trenaunay-Weber Syndrome from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
AGGF1 angiogenic factor with G patch and FHA domains 1 2.88009
KTWS Klippel-Trenaunay-Weber syndrome 2.88009