Concept information
Preferred term
Mitochondrial myopathy
Type
-
http://www.irandoc.ac.ir/onto/irandoc-meta/Concept
Broader concept
Narrower concepts
- AFG3L2 (AFG3 like matrix AAA peptidase subunit 2) related spastic ataxia, myoclonic epilepsy, neuropathy syndrome
- Autosomal dominant optic atrophy plus syndrome (disorder)
- Autosomal dominant progressive external ophthalmoplegia (disorder)
- Autosomal recessive ataxia due to ubiquinone deficiency (disorder)
- Autosomal recessive optic atrophy OPA7 type
- Autosomal recessive progressive external ophthalmoplegia
- Autosomal recessive spastic ataxia type 4
- Childhood myocerebrohepatopathy spectrum (disorder)
- Chronic diarrhea with villous atrophy syndrome (disorder)
- Combined oxidative phosphorylation defect type 11
- Combined oxidative phosphorylation defect type 13 (disorder)
- Combined oxidative phosphorylation defect type 14
- Combined oxidative phosphorylation defect type 2
- Combined oxidative phosphorylation defect type 4
- Combined oxidative phosphorylation defect type 5 (disorder)
- Combined oxidative phosphorylation defect type 7 (disorder)
- Combined oxidative phosphorylation defect type 8 (disorder)
- Combined oxidative phosphorylation defect type 9 (disorder)
- Combined oxidative phosphorylation deficiency type 20 (disorder)
- COXPD10 - combined oxidative phosphorylation defect type 10
- COXPD15 - combined oxidative phosphorylation defect type 15
- COXPD17 - combined oxidative phosphorylation defect type 17
- COXPD21 - combined oxidative phosphorylation defect type 21
- Cytochrome-c oxidase deficiency
- Deficiency of ubiquinone cytochrome c oxidoreductase
- Demyelination of central nervous system co-occurrent and due to mitochondrial disease (disorder)
- Epileptic encephalopathy with global cerebral demyelination (disorder)
- Fatal mitochondrial disease due to combined oxidative phosphorylation deficiency 3 (disorder)
- Hyperuricemia, pulmonary hypertension, renal failure, alkalosis syndrome
- Infantile hypertrophic cardiomyopathy due to mitochondrial ribosomal protein L44 deficiency (disorder)
- Infantile onset spinocerebellar ataxia (disorder)
- Leukoencephalopathy, thalamus and brainstem anomalies, high lactate syndrome (disorder)
- Leukoencephalopathy with brain stem and spinal cord involvement and high lactate syndrome (disorder)
- Lipoic acid synthetase deficiency (disorder)
- Lipoyl transferase 1 deficiency (disorder)
- Liver disease co-occurrent and due to mitochondrial disorder (disorder)
- Maternally inherited cardiomyopathy and hearing loss syndrome (disorder)
- Maternally inherited mitochondrial dystonia (disorder)
- Mental retardation, epileptic seizures, hypogonadism and hypogenitalism, microcephaly, obesity syndrome (disorder)
- Mitochondrially encoded ATP synthase membrane subunit 6-related mitochondrial spastic paraplegia
- Mitochondrial metabolism defect
- Severe neonatal lactic acidosis due to NFS1-ISD11 complex deficiency (disorder)
- Zellweger-like syndrome without peroxisomal anomaly (disorder)
Is a
In other languages
-
Persian
URI
http://www.irandoc.acir/onto/irandoc/240096000
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