Melkersson–Rosenthal syndrome
GPTKB entity
Statements (23)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
syndrome
rare disease |
| gptkbp:affects |
gptkb:nervous_system
face |
| gptkbp:causedBy |
unknown
|
| gptkbp:complication |
chronic facial swelling
|
| gptkbp:eponymOf |
gptkb:Curt_Rosenthal
Ernst Melkersson |
| gptkbp:firstDescribed |
1928
|
| gptkbp:frequency |
rare
|
| gptkbp:hasOrphanetID |
ORPHA:377
|
| https://www.w3.org/2000/01/rdf-schema#label |
Melkersson–Rosenthal syndrome
|
| gptkbp:ICD-10_code |
K13.1
|
| gptkbp:inheritance |
possibly autosomal dominant
|
| gptkbp:OMIM |
155800
|
| gptkbp:symptom |
fissured tongue
orofacial swelling recurrent facial paralysis |
| gptkbp:treatment |
surgery
corticosteroids immunosuppressants |
| gptkbp:bfsParent |
gptkb:Rosenthal_syndrome
|
| gptkbp:bfsLayer |
7
|