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Biological Sciences and Healthcare, part 4

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Concept information

Clinical finding (finding) > disease > Metabolic disease > Mitochondrial myopathy > COXPD17 - combined oxidative phosphorylation defect type 17
... > Clinical finding (finding) > disease > Genetic disease > Hereditary disease > Autosomal hereditary disorder > Recessive hereditary disorder, NOS > COXPD17 - combined oxidative phosphorylation defect type 17

Preferred term

COXPD17 - combined oxidative phosphorylation defect type 17  

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

Broader concept

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Due to

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URI

http://www.irandoc.acir/onto/irandoc/775908005

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