ICD-10: G31

obsolete tuberculous encephalitis coenurosis Gamstorp-Wohlfart syndrome Charcot-Marie-Tooth disease type 3 Charcot-Marie-Tooth disease type 4 Charcot-Marie-Tooth disease type X Bowen-Conradi syndrome Brody myopathy ornithine translocase deficiency deafness-dystonia-optic neuronopathy syndrome adenylosuccinase lyase deficiency Ogden syndrome progressive relapsing multiple sclerosis achalasia microcephaly syndrome Kahrizi syndrome CHARGE syndrome Perrault syndrome spinocerebellar ataxia type 5 corpus callosum oligodendroglioma spastic ataxia 5 autosomal recessive cerebellar ataxia spinocerebellar ataxia type 2 spinocerebellar ataxia type 6 spinocerebellar ataxia type 11 spinocerebellar ataxia type 13 obsolete spinocerebellar ataxia type 16 spinocerebellar ataxia type 17 spinocerebellar ataxia type 21 spinocerebellar ataxia type 23 spinocerebellar ataxia type 25 spinocerebellar ataxia type 29 spinocerebellar ataxia type 30 spinocerebellar ataxia type 35 spinocerebellar ataxia type 37 spinocerebellar ataxia type 40 GRID2-related spinocerebellar ataxia obsolete neurological disorder obsolete peripheral neuropathy dentatorubral-pallidoluysian atrophy gamma-amino butyric acid metabolism disorder homocarnosinosis amyotrophic lateral sclerosis type 13 amyotrophic lateral sclerosis type 15 amyotrophic lateral sclerosis type 16 amyotrophic lateral sclerosis type 19 amyotrophic lateral sclerosis type 20 Van Maldergem syndrome pontocerebellar hypoplasia pontocerebellar hypoplasia type 2A pontocerebellar hypoplasia type 3 pontocerebellar hypoplasia type 4 pontocerebellar hypoplasia type 10 Ohdo syndrome Vici syndrome Joubert syndrome with orofaciodigital defect chromosome 17p13.1 deletion syndrome Mowat-Wilson syndrome Perry syndrome Kufor-Rakeb syndrome spinal disease Ritscher-Schinzel syndrome 3MC syndrome 2 obsolete hereditary motor and sensory neuropathy with agenesis of the corpus callosum EEC syndrome hypomyelinating leukodystrophy 13