ICD-10: R94.02

chromosome 1q21.1 duplication syndrome Pitt-Hopkins syndrome Kufor-Rakeb syndrome familial temporal lobe epilepsy 6 hypomyelinating leukodystrophy obsolete Herpes simplex virus encephalitis periventricular nodular heterotopia West syndrome Athabaskan brainstem dysgenesis syndrome neonatal period electroclinical syndrome infancy electroclinical syndrome ataxia with oculomotor apraxia type 1 non-syndromic X-linked intellectual disability Meckel syndrome obsolete Opitz-GBBB syndrome achalasia microcephaly syndrome glioblastoma mesenchymal subtype Kahrizi syndrome cranio-facial dystonia spinocerebellar ataxia type 13 spinocerebellar ataxia type 21 spinocerebellar ataxia type 23 benign familial infantile epilepsy amyotrophic lateral sclerosis type 10 Van Maldergem syndrome pontocerebellar hypoplasia pontocerebellar hypoplasia type 2A pontocerebellar hypoplasia type 2B pontocerebellar hypoplasia type 6 pontocerebellar hypoplasia type 10 syndromic X-linked intellectual disability Vici syndrome Joubert syndrome with orofaciodigital defect chromosome 14q11-q22 deletion syndrome chromosome 3q29 microdeletion syndrome