Olivopontocerebellar degeneration - analogs
| Description «Olivopontocerebellar degeneration» | ||||||
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- 69% Compare Machado-Joseph Disease
- 64% Compare Binswanger atherosclerotic encephalopathy
- 58% Compare Cerebellar dysarthria
- 58% Compare Friedreich 's familial ataxia
- 57% Compare Neuroleptic syndrome
- 56% Compare Medicinal parkinsonism
- 55% Compare Corticobasal degeneration
- 54% Compare Hereditary cerebellar ataxia of Pierre-Marie
- 54% Compare Abasia
- 53% Compare Alien hand syndrome
- 53% Compare Gaye-Wernicke syndrome
- 51% Compare Spinocerebellar ataxia
- 51% Compare Strumpel 's disease
- 51% Compare Lesh-Nihan syndrome
- 46% Compare Mowgli syndrome
- 46% Compare Progressive bulbar paralysis
- 46% Compare Pseudobulbar dysarthria
- 45% Compare Dementia with Lewy bodies
- 45% Compare Secondary parkinsonism
- 45% Compare Hashimoto 's encephalopathy
- 44% Compare Primary progressive aphasia
- 44% Compare Torsion dystonia
- 44% Compare Muscular dystonia
- 44% Compare Hepatic encephalopathy
- 44% Compare Schilder 's leukoencephalitis
- 43% Compare Bulbar dysarthria
- 43% Compare Alternating syndromes
- 43% Compare Adenovirus encephalitis
- 42% Compare Lawrence-Moon-Bardet-Bidl syndrome
- 42% Compare Myoclonic dystonia
- 40% Compare Manganese poisoning
- 40% Compare Central pontine myelinolysis
- 40% Compare Acoustic-mnestic aphasia
- 39% Compare F04 Organic amnesic syndrome, not induced by alcohol and other psychoactive substances
- 38% Compare Посттравматическое стрессовое расстройство у детей
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- 38% Compare Art Syndrome
- 38% Compare Goldman-Favre disease
- 38% Compare Alcoholic myopathy
- 37% Compare A81.1 Subacute sclerosing panencephalitis
- 37% Compare Creutzfeldt-Jakob disease
- 37% Compare Athetosis
- 37% Compare Neuroleptic extrapyramidal disorders
- 36% Compare Acoustic-gnostic aphasia
- 36% Compare Ataxic cerebral palsy
- 35% Compare Anosognosia
- 35% Compare Frontal syndrome
- 35% Compare Locked-in syndrome
- 35% Compare Lethargic encephalitis
- 35% Compare Huntington's disease
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