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Congenital muscular dystrophy NOS
Congenital muscular dystrophy type 1B
Congenital muscular dystrophy with hyperlaxity
DMD
Disease central core
Duchenne muscular dystrophy
Duchenne type muscular dystrophy
Duchenne's muscular dystrophy
Eichhorst type
MD
Meryon's disease
Minicore
Multicore
Muscular dystrophy
Muscular dystrophy - Duchenne type
Nemaline
Progressive muscular dystrophy
Progressive muscular dystrophy Eichhorst
Pseudohypertrophic muscular dystrophy
Salih congenital muscular dystrophy

Vertaling van "Congenital muscular dystrophy NOS " (Engels → Nederlands) :

TERMINOLOGIE
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]
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 type 1B
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
CMD1B - congenital muscular dystrophy type 1B
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]
Salih congenital muscular dystrophy
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
vroege aanvang myopathie met fatale cardiomyopathie
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
https://browser.ihtsdotools.or (...) [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
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
http://iate.europa.eu/FindTerm (...) [HTML] [2017-12-31]
muscular dystrophy | MD [Abbr.]
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
spierdystrofie
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
http://iate.europa.eu/FindTerm (...) [HTML] [2017-12-31]
IN-CONTEXT TRANSLATIONS
List of pilot European Reference Networks for Rare Diseases · Dyscerne: European Network of Centres of Reference for Dysmorphology · ECORN CF: European Centres of Reference Network for Cystic Fibrosis · PAAIR: Patient Associations and Alpha1 International Registry, · EPNET European Porphyria Network, · EN-RBD European Network of Rare Bleeding Disorders, Paediatric Hodgkins Lymphoma Network · NEUROPED: European Network of Reference for Rare Paediatric Neurological Diseases · EURO HISTIO NET: A reference network for Langerhans cell histiocytosis and associated syndrome in EU · TAG: Together Against Genodermatoses · CARE NMD: Dissemination and Implementation of the Standards of Care for Duchene muscular ...[+++]
http://eur-lex.europa.eu/legal (...) (...) [HTML] [2013-12-31]
Overzicht van Europese proefreferentienetwerken inzake zeldzame ziekten · Dyscerne: Europees netwerk van referentiecentra voor dysmorfologie (European Network of Centres of Reference for Dysmorphology) · ECORN CF: Europees netwerk van referentiecentra voor taaislijmziekte (European Centres of Reference Network for Cystic Fibrosis) · PAAIR: Internationaal register van patiëntenverenigingen en Alpha1 (Patient Associations and Alpha1 International Registry) · EPNET: Europees porfyrienetwerk · EN-RBD: Europees Netwerk voor zeldzame bloedaandoeningen, netwerk van Hodgkin lymfoom bij kinderen (European Network of Rare Bleeding Disorders, Paediatric Hodgkins Lymphoma Network) · NEUROPED: Europees netwerk voor zeldzame neurologische aandoeningen bi ...[+++]
http://eur-lex.europa.eu/legal (...) (...) [HTML] [2013-12-31]
http://eur-lex.europa.eu/legal (...) [HTML] [2013-12-31]
breeding animals with genetic disorders that are expected to experience severe and persistent impairment of general condition, for example Huntington’s disease, Muscular dystrophy, chronic relapsing neuritis models.
https://eur-lex.europa.eu/lega (...) (...) [HTML] [2010-09-21]
Het fokken van dieren met genetische afwijkingen die naar verwachting de algemene toestand van het dier ernstig en permanent zullen hinderen, bijvoorbeeld de ziekte van Huntington, musculaire dystrofie, modellen voor terugkerende neuritis.
https://eur-lex.europa.eu/lega (...) (...) [HTML] [2010-09-21]
https://eur-lex.europa.eu/lega (...) [HTML] [2010-09-21]
breeding animals with genetic disorders that are expected to experience severe and persistent impairment of general condition, for example Huntington’s disease, Muscular dystrophy, chronic relapsing neuritis models;
http://eur-lex.europa.eu/legal (...) (...) [HTML] [2009-12-31]
Het fokken van dieren met genetische afwijkingen die naar verwachting de algemene toestand van het dier ernstig en permanent zullen hinderen, bijvoorbeeld de ziekte van Huntington, musculaire dystrofie, modellen voor terugkerende neuritis;
http://eur-lex.europa.eu/legal (...) (...) [HTML] [2009-12-31]
http://eur-lex.europa.eu/legal (...) [HTML] [2009-12-31]
List of pilot European Reference Networks for Rare Diseases · Dyscerne: European Network of Centres of Reference for Dysmorphology · ECORN CF: European Centres of Reference Network for Cystic Fibrosis · PAAIR: Patient Associations and Alpha1 International Registry, · EPNET European Porphyria Network, · EN-RBD European Network of Rare Bleeding Disorders, Paediatric Hodgkins Lymphoma Network · NEUROPED: European Network of Reference for Rare Paediatric Neurological Diseases · EURO HISTIO NET: A reference network for Langerhans cell histiocytosis and associated syndrome in EU · TAG: Together Against Genodermatoses · CARE NMD: Dissemination and Implementation of the Standards of Care for Duchene muscular ...[+++]
https://eur-lex.europa.eu/lega (...) (...) [HTML] [2009-06-07]
Overzicht van Europese proefreferentienetwerken inzake zeldzame ziekten · Dyscerne: Europees netwerk van referentiecentra voor dysmorfologie (European Network of Centres of Reference for Dysmorphology) · ECORN CF: Europees netwerk van referentiecentra voor taaislijmziekte (European Centres of Reference Network for Cystic Fibrosis) · PAAIR: Internationaal register van patiëntenverenigingen en Alpha1 (Patient Associations and Alpha1 International Registry) · EPNET: Europees porfyrienetwerk · EN-RBD: Europees Netwerk voor zeldzame bloedaandoeningen, netwerk van Hodgkin lymfoom bij kinderen (European Network of Rare Bleeding Disorders, Paediatric Hodgkins Lymphoma Network) · NEUROPED: Europees netwerk voor zeldzame neurologische aandoeningen bi ...[+++]
https://eur-lex.europa.eu/lega (...) (...) [HTML] [2009-06-07]
https://eur-lex.europa.eu/lega (...) [HTML] [2009-06-07]


Anderen hebben gezocht naar : congenital muscular dystrophy type 1b     congenital muscular dystrophy with hyperlaxity     congenital muscular dystrophy nos     disease central core     duchenne muscular dystrophy     duchenne type muscular dystrophy     duchenne's muscular dystrophy     eichhorst type     fibre-type disproportion myopathy myotubular     meryon's disease     muscular dystrophy duchenne type     salih congenital muscular dystrophy     minicore     multicore     muscular dystrophy     nemaline     progressive muscular dystrophy     progressive muscular dystrophy eichhorst     pseudohypertrophic muscular dystrophy     Congenital muscular dystrophy NOS     


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