Statements (23)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
gptkb:disease
genetic disorder |
| gptkbp:affects |
lymphatic system
|
| gptkbp:cause |
increased risk of infection
skin thickening |
| gptkbp:causedBy |
genetic disorder
|
| gptkbp:diagnosedBy |
clinical evaluation
genetic testing |
| https://www.w3.org/2000/01/rdf-schema#label |
hereditary lymphedema
|
| gptkbp:ICD-10_code |
Q82.0
|
| gptkbp:inheritance |
autosomal dominant trait
autosomal recessive trait |
| gptkbp:OMIM |
153100
|
| gptkbp:onset |
puberty
birth |
| gptkbp:subspecies |
gptkb:Milroy_disease
Meige disease |
| gptkbp:symptom |
swelling of limbs
|
| gptkbp:treatment |
surgery
physical therapy compression therapy |
| gptkbp:bfsParent |
gptkb:VEGFR3
|
| gptkbp:bfsLayer |
6
|