Statements (33)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
rare disease
vascular disorder |
| gptkbp:affects |
gptkb:skin
limbs blood vessels lymphatic vessels |
| gptkbp:alsoKnownAs |
gptkb:KTS
Klippel-Trenaunay-Weber syndrome |
| gptkbp:associatedWith |
PIK3CA gene mutation
|
| gptkbp:causedBy |
genetic disorder
|
| gptkbp:complication |
bleeding
infection pulmonary embolism deep vein thrombosis |
| gptkbp:firstDescribed |
gptkb:Maurice_Klippel
gptkb:Paul_Trénaunay 1900 |
| https://www.w3.org/2000/01/rdf-schema#label |
Klippel-Trenaunay syndrome
|
| gptkbp:inheritance |
sporadic
|
| gptkbp:isClassifiedUnder |
congenital vascular malformations
|
| gptkbp:isNotTheSameAs |
gptkb:Parkes_Weber_syndrome
|
| gptkbp:prevalence |
1 in 100,000
|
| gptkbp:symptom |
bone hypertrophy
port-wine stain soft tissue hypertrophy varicose veins |
| gptkbp:treatment |
gptkb:drug
surgery laser therapy compression therapy sclerotherapy |
| gptkbp:bfsParent |
gptkb:Parkes_Weber_syndrome
|
| gptkbp:bfsLayer |
7
|