Multiple Sclerosis and Cerebellar Ataxia without CC/MCC

Principal diagnosis codes (31)

• G11.0Congenital nonprogressive ataxia
• G11.10Early-onset cerebellar ataxia, unspecified
• G11.11Friedreich ataxia
• G11.19Other early-onset cerebellar ataxia
• G11.2Late-onset cerebellar ataxia
• G11.3Cerebellar ataxia with defective DNA repair
• G11.4Hereditary spastic paraplegia
• G11.5Hypomyelination - hypogonadotropic hypogonadism - hypodontia
• G11.6Leukodystrophy with vanishing white matter disease
• G11.8Other hereditary ataxias
• G11.9Hereditary ataxia, unspecified
• G32.81Cerebellar ataxia in diseases classified elsewhere
• G35.ARelapsing-remitting multiple sclerosis
• G35.B0Primary progressive multiple sclerosis, unspecified
• G35.B1Active primary progressive multiple sclerosis
• G35.B2Non-active primary progressive multiple sclerosis
• G35.C0Secondary progressive multiple sclerosis, unspecified
• G35.C1Active secondary progressive multiple sclerosis
• G35.C2Non-active secondary progressive multiple sclerosis
• G35.DMultiple sclerosis, unspecified
• G36.0Neuromyelitis optica [Devic]
• G36.1Acute and subacute hemorrhagic leukoencephalitis [Hurst]
• G36.8Other specified acute disseminated demyelination
• G36.9Acute disseminated demyelination, unspecified
• G37.0Diffuse sclerosis of central nervous system
• G37.1Central demyelination of corpus callosum
• G37.2Central pontine myelinolysis
• G37.5Concentric sclerosis [Balo] of central nervous system
• G37.81Myelin oligodendrocyte glycoprotein antibody disease
• G37.89Other specified demyelinating diseases of central nervous system
• G37.9Demyelinating disease of central nervous system, unspecified