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.

Descriptor ID	D007715
MeSH Number(s)	C14.907.077.410
Concept/Terms	Klippel-Trenaunay-Weber Syndrome Klippel-Trenaunay-Weber Syndrome Klippel Trenaunay Weber Syndrome Syndrome, Klippel-Trenaunay-Weber Klippel Trenaunay Syndrome Syndrome, Klippel Trenaunay Klippel-Trenaunay Syndrome Klippel-Trenaunay Syndromes Syndrome, Klippel-Trenaunay Syndromes, Klippel-Trenaunay Klippel-Trénaunay-Weber Syndrome Klippel Trénaunay Weber Syndrome Syndrome, Klippel-Trénaunay-Weber Angioosteohypertrophy Syndrome Angioosteohypertrophy Syndromes Syndrome, Angioosteohypertrophy Syndromes, Angioosteohypertrophy Klippel-Trenaunay Disease Disease, Klippel-Trenaunay Klippel Trenaunay Disease

Below are MeSH descriptors whose meaning is more general than "Klippel-Trenaunay-Weber Syndrome".

Below are MeSH descriptors whose meaning is related to "Klippel-Trenaunay-Weber Syndrome".

Below are MeSH descriptors whose meaning is more specific than "Klippel-Trenaunay-Weber Syndrome".