Statements (19)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
syndrome
|
| gptkbp:causedBy |
chromosomal deletion
genetic abnormality mutation in MAGEL2 gene mutation in SNORD116 gene |
| gptkbp:differentialDiagnosis |
gptkb:Prader-Willi_syndrome
|
| gptkbp:field |
medical genetics
|
| https://www.w3.org/2000/01/rdf-schema#label |
Prader-Willi-like syndrome
|
| gptkbp:similarTo |
gptkb:Prader-Willi_syndrome
|
| gptkbp:symptom |
obesity
hypotonia intellectual disability developmental delay hyperphagia |
| gptkbp:treatment |
behavioral therapy
dietary management growth hormone therapy |
| gptkbp:bfsParent |
gptkb:SIM1
|
| gptkbp:bfsLayer |
6
|