skip to main content

Content language

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

Concept information

Clinical finding (finding) > disease > Metabolic disease > Mitochondrial myopathy > Epileptic encephalopathy with global cerebral demyelination (disorder)
... > Clinical finding (finding) > disease > Disease of head > Disease of brain > Seizure disorder > epilepsy > Generalized epilepsy > Epileptic encephalopathy (disorder) > Epileptic encephalopathy with global cerebral demyelination (disorder)
... > Clinical finding (finding) > disease > Genetic disease > Hereditary disease > Autosomal hereditary disorder > Recessive hereditary disorder, NOS > Epileptic encephalopathy with global cerebral demyelination (disorder)
... > Clinical finding (finding) > disease > Disease of head > Disease of brain > Congenital anomaly of brain > Congenital anomaly of cerebrum (disorder) > Epileptic encephalopathy with global cerebral demyelination (disorder)

Preferred term

Epileptic encephalopathy with global cerebral demyelination (disorder)  

Type

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

Associated morphology

Finding site

Occurrence

URI

http://www.irandoc.acir/onto/irandoc/726702005

Download this concept: