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زبان محتوا

پشتیبانی: 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)

اصطلاح مرجح

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

نوع

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

به دلیل

محل یافتن

هست یک

وقوع

URI

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

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