ICD-10: G96

Other disorders of central nervous system

Related Diseases

autosomal dominant nocturnal frontal lobe epilepsy autosomal dominant nocturnal frontal lobe epilepsy 3 autosomal dominant nocturnal frontal lobe epilepsy 5 familial temporal lobe epilepsy 1 familial temporal lobe epilepsy 6 adult-onset autosomal dominant demyelinating leukodystrophy hypomyelinating leukodystrophy hypomyelinating leukodystrophy 12 syndromic X-linked intellectual disability 17 syndromic X-linked intellectual disability 7 Miles-Carpenter syndrome syndromic X-linked intellectual disability Chudley-Schwartz type obsolete West Nile virus neurological syndrome sensory system disease obsolete trivittatus encephalitis obsolete inkoo encephalitis obsolete Epstein-Barr virus encephalitis obsolete coxsackievirus encephalitis obsolete Balamuthia mandrillaris infectious disease obsolete Acanthamoeba infectious disease primary amebic meningoencephalitis obsolete tick paralysis obsolete Streptococcus agalactiae meningitis obsolete tertiary syphilitic encephalitis obsolete tertiary syphilitic meningitis obsolete Banna virus encephalitis spinal polio obsolete Lymphocytic choriomeningitis virus meningitis obsolete Lymphocytic choriomeningitis virus meningoencephalitis Walker-Warburg syndrome Askin's tumor anauxetic dysplasia 1 Bamforth-Lazarus syndrome spastic cerebral palsy Athabaskan brainstem dysgenesis syndrome ARC syndrome glioblastoma proneural subtype Kahrizi syndrome segmental dystonia oculogyric crisis Koolen de Vries syndrome infantile cerebellar-retinal degeneration brain stem medulloblastoma sacrum chordoma medulloblastoma cervical neuroblastoma spinocerebellar ataxia type 2 spinocerebellar ataxia type 4 spinocerebellar ataxia type 7 spinocerebellar ataxia type 8 spinocerebellar ataxia type 10 spinocerebellar ataxia type 11 spinocerebellar ataxia type 14 obsolete spinocerebellar ataxia type 16 spinocerebellar ataxia type 17 spinocerebellar ataxia type 18 spinocerebellar ataxia type 23 spinocerebellar ataxia type 25 spinocerebellar ataxia type 26 spinocerebellar ataxia type 28 spinocerebellar ataxia type 29 spinocerebellar ataxia type 31 cortical deafness topographical agnosia Kennedy's disease gamma-amino butyric acid metabolism disorder amyotrophic lateral sclerosis type 10 amyotrophic lateral sclerosis type 12 amyotrophic lateral sclerosis type 13 amyotrophic lateral sclerosis type 15 amyotrophic lateral sclerosis type 16 amyotrophic lateral sclerosis type 18 amyotrophic lateral sclerosis type 19 amyotrophic lateral sclerosis type 20 amyotrophic lateral sclerosis type 21 frontotemporal dementia and/or amyotrophic lateral sclerosis 1 Van Maldergem syndrome pontocerebellar hypoplasia type 1A pontocerebellar hypoplasia type 1B pontocerebellar hypoplasia type 2C pontocerebellar hypoplasia type 2E pontocerebellar hypoplasia type 3 pontocerebellar hypoplasia type 6 pontocerebellar hypoplasia type 10 Galloway-Mowat syndrome 1 Parkinson's disease 15 chromosome 14q11-q22 deletion syndrome chromosome 15q25 deletion syndrome chromosome 16p12.1 deletion syndrome chromosome 17p13.3 duplication syndrome Barber-Say syndrome ataxia with oculomotor apraxia type 3 Ritscher-Schinzel syndrome 2 Yunis-Varon syndrome ethylmalonic encephalopathy cerebral cavernous malformation spinocerebellar ataxia type 34 spinocerebellar ataxia type 35 spinocerebellar ataxia type 36 spinocerebellar ataxia type 38 spinocerebellar ataxia type 40 hypomyelinating leukoencephalopathy episodic ataxia type 5 episodic ataxia type 8 cerebellar ataxia, mental retardation and dysequlibrium syndrome autosomal recessive spinocerebellar ataxia 10 recombinase activating gene 2 deficiency obsolete neurological disorder obsolete sideroblastic anemia with spinocerebellar ataxia amusia apperceptive agnosia associative agnosia

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