ICD-10: G93

obsolete Jamestown Canyon encephalitis obsolete inkoo encephalitis obsolete polioencephalitis Frasier syndrome meningovascular neurosyphilis obsolete tertiary syphilitic meningitis obsolete infantile onset spinocerebellar ataxia biotin-responsive basal ganglia disease Athabaskan brainstem dysgenesis syndrome neonatal period electroclinical syndrome obsolete nonsyndromic epilepsy spinocerebellar ataxia with axonal neuropathy 2 choreaacanthocytosis progressive relapsing multiple sclerosis achalasia microcephaly syndrome cerebral creatine deficiency syndrome oculogyric crisis diabetic encephalopathy fragile X-associated tremor/ataxia syndrome spinocerebellar ataxia type 5 autosomal recessive spinocerebellar ataxia 10 dropped head syndrome autism spectrum disorder obsolete benign glioma brain glioma nervous system benign neoplasm autotopagnosia form agnosia integrative agnosia dentatorubral-pallidoluysian atrophy spinocerebellar ataxia type 20 spinocerebellar ataxia type 25 spinocerebellar ataxia type 27 spinocerebellar ataxia type 29 spinocerebellar ataxia type 34 spinocerebellar ataxia type 35 spinocerebellar ataxia type 37 spinocerebellar ataxia type 40 episodic ataxia type 6 episodic ataxia type 8 corpus callosum oligodendroglioma spastic ataxia 3 spastic ataxia 5 spastic ataxia 7 spinocerebellar ataxia type 6 spinocerebellar ataxia type 4 spinocerebellar ataxia type 10 spinocerebellar ataxia type 12 spinocerebellar ataxia type 14 spinocerebellar ataxia type 19/22 Kleine-Levin syndrome GABA aminotransferase deficiency succinic semialdehyde dehydrogenase deficiency amyotrophic lateral sclerosis type 12 amyotrophic lateral sclerosis type 15 amyotrophic lateral sclerosis type 20 amyotrophic lateral sclerosis type 21 pontocerebellar hypoplasia pontocerebellar hypoplasia type 2A pontocerebellar hypoplasia type 3 pontocerebellar hypoplasia type 4 pontocerebellar hypoplasia type 6 pontocerebellar hypoplasia type 10 autosomal dominant intellectual developmental disorder autosomal recessive intellectual developmental disorder amyotrophic lateral sclerosis type 22 chromosome 1p36 deletion syndrome chromosome 2q31.1 duplication syndrome chromosome 5p13 duplication syndrome autosomal dominant nocturnal frontal lobe epilepsy 2 hypomyelinating leukodystrophy hypomyelinating leukodystrophy 10 hypomyelinating leukodystrophy 12 syndromic X-linked intellectual disability Lubs type syndromic X-linked intellectual disability 17 syndromic X-linked intellectual disability Siderius type syndromic X-linked intellectual disability 34 syndromic X-linked intellectual disability 14 familial temporal lobe epilepsy 2