Inborn mitochondrial myopathy
Inborn mitochondrial myopathy
Definition
Myopathy caused by mitochondrial abnormalities.
Also known as mitochondrial myopathy — per MONDO
Also identified as
- DOID 699 per MONDO
- MESH D017240 per MONDO
- NCIT C101328 per MONDO
- Orphanet 206966 per MONDO
- UMLS C0162670 per MONDO
Affected Organs
| Organ | Involvement | Source |
|---|---|---|
| Musculature | Disease Has Associated Anatomic Site | NCIT · CC BY 4.0 |
| Musculature | Disease Has Primary Anatomic Site | NCIT · CC BY 4.0 |
| Musculoskeletal system | Disease Has Associated Anatomic Site | NCIT · CC BY 4.0 |
| Musculoskeletal system | Disease Has Primary Anatomic Site | NCIT · CC BY 4.0 |