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Becker
Benign
Benign scapuloperoneal with early contractures
Congenital muscular dystrophy NOS
Congenital muscular dystrophy type 1B
Congenital muscular dystrophy type 1B
DMD
Disease central core
Distal
Duchenne
Duchenne muscular dystrophy
Duchenne type muscular dystrophy
Duchenne's muscular dystrophy
Eichhorst type
Emery-Dreifuss
Facioscapulohumeral
Limb-girdle
Meryon's disease
Minicore
Multicore
Muscular dystrophy - Duchenne type
Nemaline
Ocular
Oculopharyngeal
Progressive muscular dystrophy
Progressive muscular dystrophy Eichhorst
Pseudohypertrophic muscular dystrophy
Scapuloperoneal
Severe

Vertaling van "Congenital muscular dystrophy type 1B " (Engels → Nederlands) :

Congenital muscular dystrophy type 1B (disorder)
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
congenitale spierdystrofie type 1B
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]
Congenital muscular dystrophy type 1B
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CMD1B - congenital muscular dystrophy type 1B
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]
Autosomal dominant limb girdle muscular dystrophy type 1B
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autosomaal dominante limb-girdle-spierdystrofie type 1B
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]
Congenital muscular dystrophy:NOS | with specific morphological abnormalities of the muscle fibre | Disease:central core | minicore | multicore | Fibre-type disproportion Myopathy:myotubular (centronuclear) | nemaline
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
central-core-disease | congenitale spierdystrofie | NNO | congenitale spierdystrofie | met specifieke morfologische-afwijkingen van spiervezel | fibre-type disproportion | minicore disease | multicore disease | myopathie | myotubulair (centronucleair) | myopathie | nemaline lichaampjes
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
https://terminologie.nictiz.nl (...) [HTML] [2018-01-01]
Duchenne muscular dystrophy | Duchenne type muscular dystrophy | Duchenne's muscular dystrophy | Meryon's disease | Muscular dystrophy - Duchenne type | pseudohypertrophic muscular dystrophy | DMD [Abbr.]
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
Duchenne spierdystrofie | pseudohypertrofische musculaire dystrofie
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
http://iate.europa.eu/FindTerm (...) [HTML] [2017-12-31]
Eichhorst type | progressive muscular dystrophy | progressive muscular dystrophy Eichhorst
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
type van Eichhorst
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http://iate.europa.eu/FindTerm (...) [HTML] [2017-12-31]
Muscular dystrophy:autosomal recessive, childhood type, resembling Duchenne or Becker | benign [Becker] | benign scapuloperoneal with early contractures [Emery-Dreifuss] | distal | facioscapulohumeral | limb-girdle | ocular | oculopharyngeal | scapuloperoneal | severe [Duchenne]
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
spierdystrofie | autosomaal recessief, op kinderleeftijd, gelijkend op Duchenne of Becker | spierdystrofie | benigne [Becker] | spierdystrofie | benigne scapuloperoneaal met vroege contracturen [Emery-Dreifuss] | spierdystrofie | distaal | spierdystrofie | ernstig [Duchenne] | spierdystrofie | facioscapulohumeraal | spierdystrofie | schouder- en bekkengordel | spierdystrofie | oculair | spierdystrofie | oculofaryngeaal | spierdystrofie | scapuloperoneaal
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
https://terminologie.nictiz.nl (...) [HTML] [2018-01-01]


Anderen hebben gezocht naar : becker     congenital muscular dystrophy type 1b     congenital muscular dystrophy nos     disease central core     duchenne     duchenne muscular dystrophy     duchenne type muscular dystrophy     duchenne's muscular dystrophy     eichhorst type     emery-dreifuss     fibre-type disproportion myopathy myotubular     meryon's disease     muscular dystrophy duchenne type     benign     benign scapuloperoneal with early contractures     distal     facioscapulohumeral     limb-girdle     minicore     multicore     nemaline     ocular     oculopharyngeal     progressive muscular dystrophy     progressive muscular dystrophy eichhorst     pseudohypertrophic muscular dystrophy     scapuloperoneal     severe     Congenital muscular dystrophy type 1B      


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Date index: 2021-09-30
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