G11.19 OTHER EARLY-ONSET CEREBELLAR ATAXIA

Synonyms

• Autosomal recessive posterior column ataxia and retinitis pigmentosa
• Childhood-onset autosomal recessive slowly progressive spinocerebellar ataxia
• Dyssynergia cerebellaris myoclonica
• Early onset cerebellar ataxia with essential tremor
• Early onset cerebellar ataxia with hypogonadism
• Early onset cerebellar ataxia with myoclonus
• Early onset cerebellar ataxia with retained tendon reflexes
• Early onset cerebellar ataxia with retinitis pigmentosa and optic atrophy
• Infantile onset spinocerebellar ataxia
• Infantile-onset autosomal recessive non progressive cerebellar ataxia
• Non-progressive cerebellar ataxia
• Primary cerebellar degeneration
• Progressive cerebellar tremor
• Progressive spinocerebellar ataxia with retained tendon reflexes
• Spectrin-associated autosomal recessive cerebellar ataxia
• Vestibulocerebellar ataxia
• X chromosome-linked sideroblastic anemia
• X-linked intellectual disability with ataxia and apraxia syndrome
• X-linked sideroblastic anemia with spinocerebellar ataxia
• X-linked spinocerebellar ataxia type 3
• X-linked spinocerebellar ataxia type 4

References to Index of Diseases and Injuries

The code G11.19 has the following ICD-10-CM references to the Index of Diseases and Injuries

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