mitochondrial encephalopathy
GPTKB entity
Statements (23)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
gptkb:disease
neurological disorder |
| gptkbp:affects |
gptkb:nervous_system
muscular system |
| gptkbp:causedBy |
mitochondrial DNA mutation
|
| gptkbp:hasNotableSubtype |
gptkb:MELAS_syndrome
|
| https://www.w3.org/2000/01/rdf-schema#label |
mitochondrial encephalopathy
|
| gptkbp:ICD-10_code |
gptkb:G31.82
|
| gptkbp:inheritance |
maternal inheritance
|
| gptkbp:subspecies |
mitochondrial disease
|
| gptkbp:symptom |
vomiting
headache muscle weakness hearing loss vision loss seizures stroke-like episodes |
| gptkbp:treatment |
gptkb:L-arginine
gptkb:coenzyme_Q10 anticonvulsants supportive therapy |
| gptkbp:bfsParent |
gptkb:NDUFS2
|
| gptkbp:bfsLayer |
7
|