Concept information
Preferred term
Mitochondrial myopathy
Type
-
http://www.irandoc.ac.ir/onto/irandoc-meta/Concept
Broader concept
Narrower concepts
- Auditory neuropathy, optic atrophy syndrome (disorder)
- Autosomal dominant progressive external ophthalmoplegia (disorder)
- CAGSSS - cataract, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, skeletal dysplasia syndrome
- Combined oxidative phosphorylation defect type 23
- Combined oxidative phosphorylation defect type 24
- Combined oxidative phosphorylation defect type 25 (disorder)
- Combined oxidative phosphorylation defect type 26
- Combined oxidative phosphorylation defect type 27
- Combined oxidative phosphorylation defect type 29
- Combined oxidative phosphorylation defect type 30
- COXPD28 - combined oxidative phosphorylation defect type 28
- Cytochrome-c oxidase deficiency
- Non-progressive predominantly posterior cavitating leukodystrophy with peripheral neuropathy (disorder)
- Non-syndromic mitochondrial sensorineural deafness (disorder)
- Ocular anomalies, axonal neuropathy, developmental delay syndrome
- Optic atrophy, ataxia, peripheral neuropathy, global developmental delay syndrome (disorder)
- QRSL1-related combined oxidative phosphorylation defect
Is a
In other languages
-
Persian
URI
http://www.irandoc.acir/onto/irandoc/240096000
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