Morgagni-Stewart-Morel syndrome
GPTKB entity
Statements (23)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
syndrome
rare disease |
| gptkbp:affects |
gptkb:women
|
| gptkbp:firstDescribed |
gptkb:Giovanni_Battista_Morgagni
Ferdinand Morel Roy Mackenzie Stewart |
| gptkbp:hasOrphanetID |
ORPHA:3246
|
| https://www.w3.org/2000/01/rdf-schema#label |
Morgagni-Stewart-Morel syndrome
|
| gptkbp:ICD-10_code |
E34.8
|
| gptkbp:inheritance |
autosomal dominant
sporadic |
| gptkbp:OMIM |
144250
|
| gptkbp:symptom |
obesity
headache hirsutism menstrual irregularities hyperostosis frontalis interna neuropsychiatric symptoms |
| gptkbp:synonym |
Frontal bone thickening syndrome
Hyperostosis frontalis interna syndrome |
| gptkbp:treatment |
symptomatic management
|
| gptkbp:bfsParent |
gptkb:Morgagni's_syndrome
|
| gptkbp:bfsLayer |
7
|