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AMD
Acid maltase deficiency
Amylopectinosis
Amylopectinosis brancher deficiency
Andersen disease
Andersen's disease
Brancher deficiency
Brancher enzyme deficiency
Dextrinosis
Familia
GSD IV
GSD-II
Gierke's disease
Glycogen disease
Glycogen storage disease
Glycogen storage disease
Glycogen storage disease I
Glycogen storage disease type II
Glycogen storage disease type IV
Glycogenopathy
Glycogenoses
Glycogenosis
Glycogenosis IV
Glycogenosis type II
Hepatorenal glycogenosis
Lipid storage disorders
Myopathy in glycogen storage disease
Najjar-Andersen syndrome
Pompe disease
Type 1 glycogenosis
Type I glycogen storage disease
Von Gierke's disease
Wilson's disease

Translation of "type i glycogen storage disease " (English → French) :

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
http://www.btb.termiumplus.gc. (...) (...) [HTML] [2018-01-01]
http://www.btb.termiumplus.gc. (...) [HTML] [2018-01-01]
acid maltase deficiency | glycogen storage disease type II | glycogenosis type II | Pompe disease | AMD [Abbr.] | GSD-II [Abbr.]
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
IATE - Health
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
http://iate.europa.eu/FindTerm (...) [HTML] [2017-12-31]
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
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
glycogénose avec cardiomyopathie sévère par déficit en glycogénine
SNOMEDCT-BE (disorder) / 717821004
SNOMEDCT-BE (disorder) / 717821004
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]
Myopathy in:glycogen storage disease (E74.0+) | lipid storage disorders (E75.-+)
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
Myopathie au cours d'anomalies de stockage (du) (des):glycogène (E74.0+) | lipides (E75.-+)
WORLD HEALTH ORGANIZATION ICD-10: G73.6*
WORLD HEALTH ORGANIZATION ICD-10: G73.6*
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
https://icd.who.int/browse10/2 (...) [HTML] [2018-01-01]
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*
WORLD HEALTH ORGANIZATION ICD-10: N16.3*
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
https://icd.who.int/browse10/2 (...) [HTML] [2018-01-01]
Andersen's disease [ Andersen disease | Najjar-Andersen syndrome | glycogenosis IV | glycogen storage disease type IV | GSD IV | alpha 1,4-glucan-6-glucosyl transferase deficiency | amylopectinosis brancher deficiency | brancher enzyme deficiency | brancher deficiency | amylopectinosis | familia ]
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
http://www.btb.termiumplus.gc. (...) (...) [HTML] [2018-01-01]
http://www.btb.termiumplus.gc. (...) [HTML] [2018-01-01]
Glycogen storage disease
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
Thésaurismose glycogénique
WORLD HEALTH ORGANIZATION ICD-10: E74.0
WORLD HEALTH ORGANIZATION ICD-10: E74.0
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
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
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
maladie des corps de polyglucosane de l'adulte
SNOMEDCT-BE (disorder) / 721099001
SNOMEDCT-BE (disorder) / 721099001
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]
glycogen storage disease [ glycogen disease | glycogenosis ]
http://www.btb.termiumplus.gc. (...) (...) [HTML] [2018-01-01]
glycogénose
Liver and Biliary Ducts
Foie et voies biliaires
http://www.btb.termiumplus.gc. (...) (...) [HTML] [2018-01-01]
http://www.btb.termiumplus.gc. (...) [HTML] [2018-01-01]
glycogen storage disease | glycogenosis | glycogenopathy | dextrinosis | glycogenoses
http://gdt.oqlf.gouv.qc.ca/fic (...) (...) [HTML] [2018-01-01]
glycogénose | thésaurose glycogénique | glycogénoses
biologie > génétique | médecine > sémiologie et pathologie
biologie > génétique | médecine > sémiologie et pathologie
http://gdt.oqlf.gouv.qc.ca/fic (...) (...) [HTML] [2018-01-01]
http://gdt.oqlf.gouv.qc.ca/fic (...) [HTML] [2018-01-01]


Others have searched : andersen disease    andersen's disease    gsd iv    gsd-ii    gierke's disease    glycogen storage disease    najjar-andersen syndrome    pompe disease    wilson's disease    acid maltase deficiency    amylopectinosis    amylopectinosis brancher deficiency    brancher deficiency    brancher enzyme deficiency    dextrinosis    familia    glycogen disease    glycogen storage disease type ii    glycogen storage disease type iv    glycogenopathy    glycogenoses    glycogenosis    glycogenosis iv    glycogenosis type ii    hepatorenal glycogenosis    lipid storage disorders    type 1 glycogenosis    type i glycogen storage disease    von gierke's disease    


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'type i glycogen storage disease'

Date index:2023-04-08 -

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