skip to main content

Biological Sciences and Healthcare, part 4

Content language

Contact us: CRM@email.irandoc.ac.ir

Concept information

Clinical finding (finding) > disease > Metabolic disease > Mitochondrial myopathy > COXPD21 - combined oxidative phosphorylation defect type 21
... > Clinical finding (finding) > disease > Genetic disease > Hereditary disease > Autosomal hereditary disorder > Recessive hereditary disorder, NOS > COXPD21 - combined oxidative phosphorylation defect type 21

Preferred term

COXPD21 - combined oxidative phosphorylation defect type 21  

Type

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

Broader concept

Is a

In other languages

URI

http://www.irandoc.acir/onto/irandoc/763211004

Download this concept:

RDF/XML TURTLE JSON-LD