Related Conditions
Mitochondrial-lipid-glycogen storage myopathy(child)
Juvenile myopathy AND lactate acidosis(child)
Mitochondrial encephalomyopathy(child)
Maternally inherited mitochondrial cardiomyopathy and myopathy(child)
Mitochondrial encephalocardiomyopathy due to transmembrane protein 70 mutation(child)
Sengers syndrome(child)
Mitochondrial myopathy with sideroblastic anemia syndrome(child)
Adult-onset chronic progressive external ophthalmoplegia with mitochondrial myopathy(child)
Pure mitochondrial myopathy(child)
Mitochondrial myopathy, lactic acidosis, deafness syndrome(child)
Adult-onset multiple mitochondrial DNA deletion syndrome due to DGUOK deficiency(child)
Progressive external ophthalmoplegia, myopathy, emaciation syndrome(child)
Lethal infantile mitochondrial myopathy(child)
Hypertrophic cardiomyopathy and renal tubular disease due to mitochondrial deoxyribonucleic acid mutation(child)
Congenital cataract, progressive muscular hypotonia, hearing loss, developmental delay syndrome(child)
Childhood-onset spasticity with hyperglycinaemia(child)
Periodic paralysis with later-onset distal motor neuropathy(child)
Mitochondrial DNA deletion syndrome with limb-girdle weakness(child)
Myopathy and diabetes mellitus(child)
Mitochondrial myopathy with reversible cytochrome C oxidase deficiency(child)
Quick Facts
- SNOMED CT
- 16851005
- UMLS CUI
- C0162670
- Fully Specified Name
- Mitochondrial myopathy (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
Medical Disclaimer
This information is for educational purposes only and does not constitute medical advice, diagnosis, or treatment. Always consult with a qualified healthcare provider regarding any medical condition or treatment plan.
Clinical content is derived from the SNOMED CT clinical ontology and curated medical knowledge graphs.