A rare mitochondrial disease with characteristics of adult onset of progressive external ophthalmoplegia, exercise intolerance, muscle weakness, manifestations of spinocerebellar ataxia (e.g. impaired gait, dysarthria) and mild motor peripheral neuro

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ophtalmoplégie externe progressive chronique de l'adulte avec myopathie mitochondriale

SNOMEDCT-BE (e.g. impaired gait, dysarthria) and mild motor peripheral neuro / 725464001

SNOMEDCT-BE (disorder) / 725464001

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A rare mitochondrial oxidative phosphorylation disorder due to nuclear deoxyribonucleic acid anomalies. The disease is characterized by progressive external ophthalmoplegia without diplopia, cerebellar atrophy, proximal skeletal muscle weakness with

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syndrome d'ophtalmoplégie externe progressive-myopathie-émaciation

SNOMEDCT-BE (disorder) / 764733009

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https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]

A rare mitochondrial oxidative phosphorylation disorder due to nuclear deoxyribonucleic acid anomalies. The disease is characterised by progressive external ophthalmoplegia without diplopia, cerebellar atrophy, proximal skeletal muscle weakness with

https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]

syndrome d'OEP-myopathie-émaciation

SNOMEDCT-BE (disorder) / 764733009

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https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]

Progressive supranuclear ophthalmoplegia [Steele-Richardson-Olszewski]

https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]

Ophtalmoplégie supranucléaire progressive [maladie de Steele-Richardson-Olszewski]

WORLD HEALTH ORGANIZATION ICD-10: G23.1

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https://icd.who.int/browse10/2 (...) [HTML] [2018-01-01]

external ophthalmoplegia