- Concept UI
- M0012064
- Scope Note
- 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.
- Terms
-
Klippel-Trenaunay-Weber Syndrome
Preferred Term
Term UI
T023153
Date01/01/1999
LexicalTag
EPO
ThesaurusID
-
Angioosteohypertrophy Syndrome
Term UI
T768970
Date04/08/2010
LexicalTag
NON
ThesaurusID
-
Congenital Dysplastic Angiopathy
Term UI
T841831
Date04/18/2013
LexicalTag
NON
ThesaurusID
NLM (2014)
-
Klippel Trenaunay Syndrome
Term UI
T768969
Date04/08/2010
LexicalTag
EPO
ThesaurusID
-
Klippel-Trenaunay Syndrome
Term UI
T811683
Date11/15/2011
LexicalTag
NON
ThesaurusID
-
Klippel-Trénaunay-Weber Syndrome
Term UI
T769310
Date04/14/2010
LexicalTag
EPO
ThesaurusID
NLM (2011)
-
KTW Syndrome
Term UI
T844342
Date05/17/2013
LexicalTag
NON
ThesaurusID
GHR (2014)
-
Angio-Osteohypertrophy Syndrome
Term UI
T841830
Date04/18/2013
LexicalTag
NON
ThesaurusID
GHR (2014)
-
Klippel-Trenaunay Disease
Term UI
T023152
Date04/01/1993
LexicalTag
EPO
ThesaurusID