Kocher-Debre-Semelaigne myopathy
GPTKB entity
Statements (17)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
gptkb:disease
gptkb:muscular_dystrophy |
| gptkbp:affects |
children
|
| gptkbp:alsoKnownAs |
gptkb:Kocher-Debre-Semelaigne_syndrome
|
| gptkbp:associatedWith |
congenital hypothyroidism
|
| gptkbp:characterizedBy |
hypothyroidism
muscular hypertrophy |
| gptkbp:firstDescribed |
gptkb:Georges_Semelaigne
gptkb:Robert_Debré gptkb:Emil_Theodor_Kocher |
| gptkbp:symptom |
muscle stiffness
muscle weakness macroglossia |
| gptkbp:treatment |
thyroid hormone replacement
|
| gptkbp:bfsParent |
gptkb:Kocher-Debre-Semelaigne_syndrome
|
| gptkbp:bfsLayer |
7
|
| http://www.w3.org/2000/01/rdf-schema#label |
Kocher-Debre-Semelaigne myopathy
|