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 Angioosteohypertrophy Syndrome Angioosteohypertrophy Syndromes Syndrome, Angioosteohypertrophy Syndromes, Angioosteohypertrophy Congenital Dysplastic Angiopathy Angiopathies, Congenital Dysplastic Angiopathy, Congenital Dysplastic Congenital Dysplastic Angiopathies Dysplastic Angiopathies, Congenital Dysplastic Angiopathy, Congenital 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 KTW Syndrome KTW Syndromes Syndrome, KTW Syndromes, KTW Angio-Osteohypertrophy Syndrome Angio Osteohypertrophy Syndrome Angio-Osteohypertrophy Syndromes Syndrome, Angio-Osteohypertrophy Syndromes, Angio-Osteohypertrophy 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".