Link to this page
Medical Subject Headings
Last uploaded:
March 22, 2026
| Id | http://purl.bioontology.org/ontology/MESH/D007715
http://purl.bioontology.org/ontology/MESH/D007715
|
|---|---|
| Preferred Name | Klippel-Trenaunay-Weber Syndrome |
| Definitions |
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.
|
| Synonyms |
Syndromes, Angio-Osteohypertrophy
Syndromes, Klippel-Trenaunay
Syndrome, Angioosteohypertrophy
Klippel-Trenaunay Syndrome
Angio-Osteohypertrophy Syndrome
Disease, Klippel-Trenaunay
Syndrome, Angio-Osteohypertrophy
Congenital Dysplastic Angiopathies
Dysplastic Angiopathy, Congenital
Congenital Dysplastic Angiopathy
Klippel-Trenaunay Disease
Syndromes, KTW
Syndrome, Klippel-Trenaunay-Weber
KTW Syndrome
Angiopathy, Congenital Dysplastic
Syndromes, Angioosteohypertrophy
Angioosteohypertrophy Syndrome
Angio-Osteohypertrophy Syndromes
Klippel Trenaunay Weber Syndrome
Dysplastic Angiopathies, Congenital
Angio Osteohypertrophy Syndrome
KTW Syndromes
Angioosteohypertrophy Syndromes
Klippel Trenaunay Disease
Klippel Trenaunay Syndrome
Klippel Trénaunay Weber Syndrome
Syndrome, Klippel-Trénaunay-Weber
Klippel-Trénaunay-Weber Syndrome
Syndrome, Klippel-Trenaunay
Klippel-Trenaunay Syndromes
Syndrome, Klippel Trenaunay
Syndrome, KTW
Angiopathies, Congenital Dysplastic
See more
See less
|
| Type | http://www.w3.org/2002/07/owl#Class |
All Properties
| 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. |
|---|---|
| altLabel |
Syndromes, Angio-Osteohypertrophy
Syndromes, Klippel-Trenaunay
Syndrome, Angioosteohypertrophy
Klippel-Trenaunay Syndrome
Angio-Osteohypertrophy Syndrome
Disease, Klippel-Trenaunay
Syndrome, Angio-Osteohypertrophy
Congenital Dysplastic Angiopathies
Dysplastic Angiopathy, Congenital
Congenital Dysplastic Angiopathy
Klippel-Trenaunay Disease
Syndromes, KTW
Syndrome, Klippel-Trenaunay-Weber
KTW Syndrome
Angiopathy, Congenital Dysplastic
Syndromes, Angioosteohypertrophy
Angioosteohypertrophy Syndrome
Angio-Osteohypertrophy Syndromes
Klippel Trenaunay Weber Syndrome
Dysplastic Angiopathies, Congenital
Angio Osteohypertrophy Syndrome
KTW Syndromes
Angioosteohypertrophy Syndromes
Klippel Trenaunay Disease
Klippel Trenaunay Syndrome
Klippel Trénaunay Weber Syndrome
Syndrome, Klippel-Trénaunay-Weber
Klippel-Trénaunay-Weber Syndrome
Syndrome, Klippel-Trenaunay
Klippel-Trenaunay Syndromes
Syndrome, Klippel Trenaunay
Syndrome, KTW
Angiopathies, Congenital Dysplastic
See more
See less
|
| prefLabel | Klippel-Trenaunay-Weber Syndrome
|
| Machine permutation | 94; was KLIPPEL-TRENAUNAY DISEASE 1975-93 (see under ANGIOMATOSIS 1975-90)
|
| HN | 94; was KLIPPEL-TRENAUNAY DISEASE 1975-93 (see under ANGIOMATOSIS 1975-90)
|
| Mapped from | |
| type | |
| tui | T047
|
| TERMUI |
T023152
T023153
T841831
T768970
T841830
T811683
T768969
T769310
T844342
See more
See less
|
| TH |
OMIM (2013)
NLM (1975)
NLM (1994)
GHR (2014)
NLM (2014)
NLM (2011)
ORD (2010)
See more
See less
|
| MMR | 20130708
|
| notation | D007715
|
| Semantic type UMLS property | |
| Inverse of AQ |
See more
See less
|
| DX | 19910101
|
| cui | C0022739
|
| DC | 1
|
| MN | C14.907.077.410
|
| AQL | BL CF CI CL CO DG DH DI DT EC EH EM EN EP ET GE HI IM ME MI MO NU PA PC PP PS PX RH RT SU TH UR VE VI
|
| OL | use KLIPPEL-TRENAUNAY-WEBER SYNDROME to search KLIPPEL-TRENAUNAY DISEASE 1975-93; search ANGIOMATOSIS 1966-74
|
| MDA | 19990101
|
| subClassOf |
| Delete | Subject | Author | Type | Created |
|---|---|---|---|---|
| No notes to display |