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Disease Klippel-Trenaunay-Weber Syndrome

Name Klippel-Trenaunay-Weber Syndrome
Synonyms Angioosteohypertrophy Syndrome | Angio Osteohypertrophy Syndrome | Angio-Osteohypertrophy Syndrome | Angioosteohypertrophy Syndromes | Angio-Osteohypertrophy Syndromes | Angiopathies, Congenital Dysplastic | Angiopathy, Congenital Dysplastic | Congenital Dysplastic Angiopathies | Congenital Dysplastic Angiopathy | Disease, Klippel-Trenaunay | Dysplastic Angiopathies, Congenital | Dysplastic Angiopathy, Congenital | Klippel Trenaunay Disease | Klippel-Trenaunay Disease | Klippel Trenaunay Syndrome | Klippel-Trenaunay Syndrome | Klippel-Trenaunay Syndromes | Klippel Trenaunay Weber Syndrome | Klippel Trénaunay Weber Syndrome | Klippel-Trénaunay-Weber Syndrome | KTS | KTW Syndrome | KTW Syndromes | Syndrome, Angioosteohypertrophy | Syndrome, Angio-Osteohypertrophy | Syndrome, Klippel Trenaunay | Syndrome, Klippel-Trenaunay | Syndrome, Klippel-Trenaunay-Weber | Syndrome, Klippel-Trénaunay-Weber | Syndrome, KTW | Syndromes, Angioosteohypertrophy | Syndromes, Angio-Osteohypertrophy | Syndromes, Klippel-Trenaunay | Syndromes, KTW
Definition A congenital disorder that is characterized by a triad of capillary malformations (HEMANGIOMA), venous malformations (ARTERIOVENOUS FISTULA), and soft tissue or bony hypertrophy of the limb. This syndrome is caused by mutations in the VG5Q gene which encodes a strong angiogenesis stimulator.
Categories Cardiovascular disease
MeSH® ID D007715
OMIM® ID 149000
External Links

Top ↑ Ancestors

DiseasesCardiovascular Diseases Has associated chemicals Has associated genes Has associated exposure references Vascular Diseases Has associated chemicals Has associated genes Has associated exposure references Angiomatosis Has associated chemicals Has associated genes Klippel-Trenaunay-Weber Syndrome Has associated chemicals Has associated genes

Top ↑ Descendants

Klippel-Trenaunay-Weber Syndrome Has associated chemicals Has associated genes
  Weber Klippel Trenaunay