Skip to contentMultiple sclerosis and cerebellar ataxia with mcc
- G11.0 Congenital nonprogressive ataxia
- G11.10 Early-onset cerebellar ataxia, unspecified
- G11.11 Friedreich ataxia
- G11.19 Other early-onset cerebellar ataxia
- G11.2 Late-onset cerebellar ataxia
- G11.3 Cerebellar ataxia with defective DNA repair
- G11.4 Hereditary spastic paraplegia
- G11.5 Hypomyelination – hypogonadotropic hypogonadism – hypodontia
- G11.6 Leukodystrophy with vanishing white matter disease
- G11.8 Other hereditary ataxias
- G11.9 Hereditary ataxia, unspecified
- G32.81 Cerebellar ataxia in diseases classified elsewhere
- G35 Multiple sclerosis
- G36.0 Neuromyelitis optica [Devic]
- G36.1 Acute and subacute hemorrhagic leukoencephalitis [Hurst]
- G36.8 Other specified acute disseminated demyelination
- G36.9 Acute disseminated demyelination, unspecified
- G37.0 Diffuse sclerosis of central nervous system
- G37.1 Central demyelination of corpus callosum
- G37.2 Central pontine myelinolysis
- G37.5 Concentric sclerosis [Balo] of central nervous system
- G37.81 Myelin oligodendrocyte glycoprotein antibody disease
- G37.89 Other specified demyelinating diseases of central nervous system
- G37.9 Demyelinating disease of central nervous system, unspecified
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