Statements (32)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
syndrome
rare disease |
| gptkbp:affects |
gptkb:skin
blood vessels lymphatic system |
| gptkbp:associatedWith |
gptkb:PIK3CA_gene
|
| gptkbp:causedBy |
genetic disorder
|
| gptkbp:complication |
bleeding
infection pulmonary embolism deep vein thrombosis |
| gptkbp:distinctFrom |
gptkb:Parkes_Weber_syndrome
|
| gptkbp:firstDescribed |
gptkb:Maurice_Klippel
gptkb:Paul_Trénaunay 1900 |
| gptkbp:hasOrphanetID |
ORPHA:2512
|
| https://www.w3.org/2000/01/rdf-schema#label |
Klippel–Trénaunay syndrome
|
| gptkbp:ICD-10_code |
Q87.2
|
| gptkbp:onset |
congenital
|
| gptkbp:prevalence |
rare
|
| gptkbp:symptom |
bone hypertrophy
port-wine stain soft tissue hypertrophy varicose veins |
| gptkbp:synonym |
gptkb:Klippel–Trénaunay–Weber_syndrome
gptkb:KTS |
| gptkbp:treatment |
surgery
laser therapy compression therapy sclerotherapy |
| gptkbp:bfsParent |
gptkb:Klippel–Trénaunay–Weber_syndrome
|
| gptkbp:bfsLayer |
7
|