mitochondrial encephalomyopathy
GPTKB entity
Statements (26)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
gptkb:disease
gptkb:mitochondrial_disorder |
| gptkbp:affects |
gptkb:nervous_system
muscles |
| gptkbp:causedBy |
mitochondrial DNA mutation
nuclear DNA mutation |
| https://www.w3.org/2000/01/rdf-schema#label |
mitochondrial encephalomyopathy
|
| gptkbp:ICD-10_code |
gptkb:G31.82
|
| gptkbp:inheritance |
maternal inheritance
autosomal inheritance |
| gptkbp:subclassOf |
metabolic disorder
muscular dystrophy |
| gptkbp:subspecies |
gptkb:MELAS_syndrome
MERRF syndrome |
| gptkbp:symptom |
muscle weakness
seizures lactic acidosis stroke-like episodes |
| gptkbp:treatment |
physical therapy
anticonvulsants supportive therapy |
| gptkbp:bfsParent |
gptkb:ND1
gptkb:ND5 gptkb:ND6 gptkb:SUCLA2 |
| gptkbp:bfsLayer |
7
|