type I glycogen storage disease [ von Gierke's disease | Gierke's disease | type 1 glycogenosis | glycogen storage disease I | hepatorenal glycogenosis ]

http://www.btb.termiumplus.gc. (...) (...) [HTML] [2018-01-01]

maladie de von Gierke [ glycogénose de type I | glycogénose hépato-rénale ]

Liver and Biliary Ducts | Human Diseases - Various

Foie et voies biliaires | Maladies humaines diverses

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

déficit en maltase acide | glycogénose de type II | maladie de Pompe | GSD II [Abbr.]

IATE - Health

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http://www.btb.termiumplus.gc. (...) (...) [HTML] [2018-01-01]

maladie d'Andersen [ glycogénose musculaire type IV ]

Endocrine System and Metabolism | Liver and Biliary Ducts

Systèmes endocrinien et métabolique | Foie et voies biliaires

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An extremely rare genetic glycogen storage disease reported in one patient to date. Clinical signs included muscle weakness, cardiac arrhythmia associated with accumulation of abnormal storage material in the heart and glycogen depletion in skeletal

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glycogénose avec cardiomyopathie sévère par déficit en glycogénine

SNOMEDCT-BE (disorder) / 717821004

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Renal tubulo-interstitial disorders in:cystinosis (E72.0+) | glycogen storage disease (E74.0+) | Wilson's disease (E83.0+)

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

Maladie rénale tubulo-interstitielle au cours de:cystinose (E72.0+) | glycogénose (E74.0+) | maladie de Wilson (E83.0+)

WORLD HEALTH ORGANIZATION ICD-10: N16.3*

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

A glycogen storage disease of adults with characteristics of progressive upper and lower motor neuron dysfunction, progressive neurogenic bladder and cognitive difficulties that can lead to dementia. The prevalence is unknown. More than 50 cases have

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maladie des corps de polyglucosane de l'adulte

SNOMEDCT-BE (disorder) / 721099001

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

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

IATE - Agricultural activity

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goitre exophtalmique | maladie de Basedow | maladie de Flajani | maladie de Graves | maladie de Marsh

IATE - Health

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Disease with characteristics of the adult-onset (average age 40 years) of truncal ataxia, gait disturbance and gaze-evoked nystagmus. The disease is slowly progressive with dysarthria and limb ataxia following. Additional manifestations include diplo

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ataxie spinocérébelleuse type 38

SNOMEDCT-BE (average age 40 years) of truncal ataxia, gait disturbance and gaze-evoked nystagmus. The disease is slowly progressive with dysarthria and limb ataxia following. Additional manifestations include diplo / 734021001

SNOMEDCT-BE (disorder) / 734021001

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

Others have searched : andersen disease andersen's disease basedow's disease flajani's disease gsd iv gsd-ii gierke's disease graves disease graves's disease march's disease najjar-andersen syndrome parry disease parry's disease pompe disease stokes's disease wilson's disease acid maltase deficiency amylopectinosis amylopectinosis brancher deficiency blue disease blue ear disease blue-ear disease of pigs brancher deficiency brancher enzyme deficiency exophthalmic goiter familia glycogen disease glycogen storage disease glycogen storage disease type ii glycogen storage disease type iv glycogenosis glycogenosis iv glycogenosis type ii hepatorenal glycogenosis mysterious pig disease mysterious swine disease mystery pig disease new pig disease porcine epidemical abortion porcine reproductive and respiratory syndrome purple ears disease thyrotoxicosis type 1 glycogenosis type i glycogen storage disease von gierke's disease Glycogen disease

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'Glycogen disease'

Date index:2022-02-12 -

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Translation of "Glycogen disease " (English → French) :

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