Klippel-Trenaunay-Weber Syndrome Gene Set

Dataset HuGE Navigator Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description A rare congenital syndrome characterized by large cutaneous hemangiomata with hypertrophy of the related bones and soft tissues. (Human Disease Ontology, DOID_2926)
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Genes

1 genes associated with the Klippel-Trenaunay-Weber Syndrome phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

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