ICD-10: G96
Other disorders of central nervous system
Subcategories
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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