Statements (23)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
gptkb:disease
genetic disorder |
| gptkbp:affects |
lymphatic system
|
| gptkbp:alsoKnownAs |
Milroy's disease
hereditary lymphedema type I |
| gptkbp:cause |
mutation in FLT4 gene
|
| gptkbp:diagnosedBy |
clinical evaluation
genetic testing |
| gptkbp:firstDescribed |
gptkb:William_Milroy
1892 |
| https://www.w3.org/2000/01/rdf-schema#label |
Milroy disease
|
| gptkbp:inheritance |
autosomal dominant
|
| gptkbp:OMIM |
153100
|
| gptkbp:prevalence |
rare
|
| gptkbp:symptom |
thickened skin
chronic lymphedema swelling of lower limbs toenail changes |
| gptkbp:treatment |
physical therapy
skin care compression therapy |
| gptkbp:bfsParent |
gptkb:VEGFR3
|
| gptkbp:bfsLayer |
6
|