| Dataset | OMIM Gene-Disease 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) |
| External Link | http://www.omim.org/entry/149000 |
| Similar Terms | |
| Downloads & Tools |
1 genes associated with the klippel-trenaunay-weber syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
| Symbol | Name |
|---|---|
| KTWS | Klippel-Trenaunay-Weber syndrome |
