ICD-10: G98

autosomal dominant nocturnal frontal lobe epilepsy 2 autosomal dominant nocturnal frontal lobe epilepsy 4 familial temporal lobe epilepsy 1 familial temporal lobe epilepsy 2 adult-onset autosomal dominant demyelinating leukodystrophy hypomyelinating leukodystrophy 12 Prieto syndrome syndromic X-linked intellectual disability Siderius type obsolete Brooks-Wisniewski-Brown syndrome Norrie disease nervous system disease phenobarbital allergy intestinal botulism obsolete Measles virus encephalitis obsolete Rubella virus encephalitis obsolete polioencephalitis coenurosis obsolete tertiary syphilitic meningitis spinal polio obsolete Lymphocytic choriomeningitis virus meningitis Charcot-Marie-Tooth disease type X Walker-Warburg syndrome Askin's tumor alternating hemiplegia of childhood alcohol-related neurodevelopmental disorder Borjeson-Forssman-Lehmann syndrome Athabaskan brainstem dysgenesis syndrome Bowen-Conradi syndrome Brown-Vialetto-Van Laere syndrome variable age at onset electroclinical syndrome obsolete nonsyndromic epilepsy early onset absence epilepsy ornithine translocase deficiency spinocerebellar ataxia with axonal neuropathy 2 spastic ataxia 1 progressive relapsing multiple sclerosis achalasia microcephaly syndrome cerebral creatine deficiency syndrome glioblastoma proneural subtype glioblastoma mesenchymal subtype segmental dystonia cranio-facial dystonia spinocerebellar ataxia type 5 IMAGe syndrome non-syndromic intellectual disability parietal lobe ependymoma spinocerebellar ataxia type 1 spinocerebellar ataxia type 4 spinocerebellar ataxia type 10 spinocerebellar ataxia type 11 spinocerebellar ataxia type 14 spinocerebellar ataxia type 15 obsolete spinocerebellar ataxia type 16 spinocerebellar ataxia type 17 autosomal dominant cerebellar ataxia, deafness and narcolepsy spinocerebellar ataxia type 18 spinocerebellar ataxia type 21 spinocerebellar ataxia type 25 spinocerebellar ataxia type 26 spinocerebellar ataxia type 29 spinocerebellar ataxia type 34 Warburg micro syndrome Van Maldergem syndrome rippling muscle disease 2 pontocerebellar hypoplasia pontocerebellar hypoplasia type 1A pontocerebellar hypoplasia type 2A pontocerebellar hypoplasia type 3 pontocerebellar hypoplasia type 5 pontocerebellar hypoplasia type 10 CEDNIK syndrome Stormorken syndrome amyotrophic lateral sclerosis type 22 Vici syndrome chromosome 2q31.2 deletion syndrome chromosome 5q12 deletion syndrome chromosome 6q11-q14 deletion syndrome EAST syndrome Mowat-Wilson syndrome Perry syndrome Pitt-Hopkins syndrome ataxia with oculomotor apraxia type 3 Ritscher-Schinzel syndrome 2 3MC syndrome 2 lethal congenital contracture syndrome 3 cerebral cavernous malformation autosomal dominant nocturnal frontal lobe epilepsy autosomal dominant nocturnal frontal lobe epilepsy 1 spinocerebellar ataxia type 37 spinocerebellar ataxia type 40 episodic ataxia type 7 autosomal recessive spinocerebellar ataxia 10 coronin-1A deficiency dropped head syndrome cerebellar medulloblastoma nervous system benign neoplasm sensory system cancer akinetopsia associative agnosia childhood spinal muscular atrophy Kennedy's disease homocarnosinosis amyotrophic lateral sclerosis type 10 amyotrophic lateral sclerosis type 11 amyotrophic lateral sclerosis type 12 amyotrophic lateral sclerosis type 13 amyotrophic lateral sclerosis type 15 obsolete amyotrophic lateral sclerosis type 17 amyotrophic lateral sclerosis type 18 amyotrophic lateral sclerosis type 19 amyotrophic lateral sclerosis type 20