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Biological Sciences and Healthcare, part 5

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Concept information

Clinical finding (finding) > disease > Metabolic disease > Mitochondrial myopathy > Combined oxidative phosphorylation defect type 29
Hereditary cerebellar degeneration > Hereditary cerebellar atrophy (disorder) > Combined oxidative phosphorylation defect type 29

Preferred term

Combined oxidative phosphorylation defect type 29  

Type

  • http://www.irandoc.ac.ir/onto/irandoc-meta/Concept

Broader concept

Associated morphology

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Is a

Occurrence

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URI

http://www.irandoc.acir/onto/irandoc/1172843003

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