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 > Congenital disease > Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1 (disorder)
... > Clinical finding (finding) > disease > Genetic disease > Hereditary disease > Autosomal hereditary disorder > Recessive hereditary disorder, NOS > Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1 (disorder)

Preferred term

Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1 (disorder)  

Type

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

Broader concept

Due to

Finding site

Is a

Occurrence

In other languages

URI

http://www.irandoc.acir/onto/irandoc/764962002

Download this concept:

RDF/XML TURTLE JSON-LD