Jump to:
loading...| Preferred Name |
Mitochondrial cytopathy |
|
| Synonyms |
|
|
| ID |
http://www.semanticweb.org/ontologies/STO.owl#OWLClass_621cd72f_5aa7_4745_a792_42567f306060 |
|
| isDefinedBy |
Mitochondrial cytopathies represent a heterogeneous group of multisystem disorders which preferentially affect the muscle and nervous systems. They are caused either by mutations in the maternally inherited mitochondrial genome, or by nuclear DNA-mutations. |
|
| label |
Mitochondrial cytopathy |
|
| prefixIRI |
OWLClass_621cd72f_5aa7_4745_a792_42567f306060 |
|
| prefLabel |
Mitochondrial cytopathy |
|
| references |
Schmiedel, J., Jackson, S., Schäfer, J., & Reichmann, H. (2003). Mitochondrial cytopathies. Journal of neurology, 250(3), 267-277. |
|
| synonyms |
Mitochondrial disease |
|
| subClassOf |
http://www.semanticweb.org/ontologies/STO.owl#OWLClass_23e71a33_674f_4315_a558_53eb2597b5d2 |
Create mapping