|Dataset||HuGE Navigator Gene-Phenotype 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|
1 genes associated with the Klippel-Trenaunay-Weber Syndrome phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
|AGGF1||angiogenic factor with G patch and FHA domains 1|