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Vertaling van "Myopathy " (Engels → Nederlands) :

A rare genetic mitochondrial oxidative phosphorylation disorder with characteristics of either late-onset myopathy with progressive external ophthalmoplegia and muscular weakness (predominantly limb-girdle) or early-onset myopathy presenting with dec

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DNA2-gerelateerd mitochondriaal DNA-deletiesyndroom

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

myopathy

http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]

myopathie | spierziekte

http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]

http://iate.europa.eu/FindTerm (...) [HTML] [2017-12-31]

nemaline myopathy

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nemaline myopathie

http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]

http://iate.europa.eu/FindTerm (...) [HTML] [2017-12-31]

myopathie

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myopathie

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http://iate.europa.eu/FindTerm (...) [HTML] [2017-12-31]

Myopathy in:hyperparathyroidism (E21.0-E21.3+) | hypoparathyroidism (E20.-+) | Thyrotoxic myopathy (E05.-+)

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

myopathie bij | hyperparathyroïdie (E21.0-E21.3) | myopathie bij | hypoparathyroïdie (E20.-) | thyrotoxische myopathie (E05.-)

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

https://terminologie.nictiz.nl (...) [HTML] [2018-01-01]

A rare genetic, non-dystrophic myopathy with characteristics of fatigable muscle weakness associated with congenital myopathy. Patients present with axial hypotonia, myopathic facies with fatigable ptosis, feeding difficulties, delayed gross motor de

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congenitale myopathie met myasthenie-achtige aanvang

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myopathy | muscle diease

http://users.ugent.be/~rvdstic (...) (...) [HTML] [2018-01-01]

myopathie | spierziekte

http://users.ugent.be/~rvdstic (...) (...) [HTML] [2018-01-01]

http://users.ugent.be/~rvdstic (...) [HTML] [2018-01-01]

Autoimmune necrotising myopathy

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auto-immune necrotiserende myopathie