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Becker
Benign
Benign scapuloperoneal with early contractures
Congenital muscular dystrophy NOS
Congenital muscular dystrophy with ITGA7 deficiency
Congenital muscular dystrophy with hyperlaxity
Disease central core
Distal
Duchenne
Emery-Dreifuss
Facioscapulohumeral
Limb-girdle
Minicore
Multicore
Nemaline
Ocular
Oculopharyngeal
Scapuloperoneal
Severe

Vertaling van "congenital muscular dystrophy with hyperlaxity " (Engels → Nederlands) :

Congenital muscular dystrophy with hyperlaxity
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
CMDH - congenital muscular dystrophy with hyperlaxity
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]
Congenital muscular dystrophy with hyperlaxity (disorder)
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
congenitale spierdystrofie met hyperlaxiteit
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]
Congenital muscular dystrophy with ITGA7 deficiency
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
congenitale spierdystrofie met integrine alfa-7-deficiëntie
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]
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 with hyperlaxity     congenital muscular dystrophy nos     disease central core     duchenne     emery-dreifuss     fibre-type disproportion myopathy myotubular     benign     benign scapuloperoneal with early contractures     distal     facioscapulohumeral     limb-girdle     minicore     multicore     nemaline     ocular     oculopharyngeal     scapuloperoneal     severe     


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Date index: 2023-01-16
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