klippel-trenaunay-weber syndrome Gene Set

Dataset GAD 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)
Similar Terms
Downloads & Tools

Genes

1 genes associated with the disease klippel-trenaunay-weber syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Symbol Name
AGGF1 angiogenic factor with G patch and FHA domains 1