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Concept information

... > Clinical finding (finding) > disease > Genetic disease > Hereditary disease > Autosomal hereditary disorder > Dominant hereditary disorder, NOS > Early-onset epileptic encephalopathy and intellectual disability due to GRIN2A mutation
... > Clinical finding (finding) > disease > mental disorder > Developmental mental disorder > Intellectual disability > Early-onset epileptic encephalopathy and intellectual disability due to GRIN2A mutation
... > Clinical finding (finding) > disease > developmental disorder > Neurodevelopmental disorder > Developmental mental disorder > Intellectual disability > Early-onset epileptic encephalopathy and intellectual disability due to GRIN2A mutation
... > Clinical finding (finding) > disease > Disease of head > Disease of brain > Seizure disorder > epilepsy > Generalized epilepsy > Symptomatic generalized epilepsy > Early-onset epileptic encephalopathy and intellectual disability due to GRIN2A mutation
... > Clinical finding (finding) > Head and neck finding > Head finding (finding) > Finding of brain > Seizure > Seizure disorder > epilepsy > Generalized epilepsy > Symptomatic generalized epilepsy > Early-onset epileptic encephalopathy and intellectual disability due to GRIN2A mutation

Preferred term

Early-onset epileptic encephalopathy and intellectual disability due to GRIN2A mutation  

Type

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

Finding site

Occurrence

URI

http://www.irandoc.acir/onto/irandoc/770431001

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