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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glycogenosis

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glycogénose

IATE - Health

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

Forbes glycogenosis

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maladie de Forbes

IATE - Health

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

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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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macular corneal dystrophy [ macular dystrophy | Groenouw's macular type II corneal dystrophy | Groenouw type II corneal dystrophy | Bückler's type II corneal dystrophy | Fehr's spotted corneal dystrophy ]

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dystrophie maculaire [ dystrophie de Groenouw type II ]

Visual Disorders

Troubles de la vision

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Atrioventricular block, type I and II Möbitz block, type I and II Second-degree block, type I and II Wenckebach's block

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

Bloc (de) (du):auriculoventriculaire, type I et II | Möbitz, type I et II | second degré, type I et II | Wenckebach

WORLD HEALTH ORGANIZATION ICD-10: I44.1

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

touch type | type quickly | type at speed | typing at speed

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taper vite

skill

Aptitude

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Progressive bulbar palsy of childhood [Fazio-Londe] Spinal muscular atrophy:adult form | childhood form, type II | distal | juvenile form, type III [Kugelberg-Welander] | scapuloperoneal form

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WORLD HEALTH ORGANIZATION ICD-10: G12.1

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Anaemia:haemolytic nonspherocytic (hereditary), type II | hexokinase deficiency | pyruvate kinase [PK] deficiency | triose-phosphate isomerase deficiency

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

Anémie (due à):déficit en:hexokinase | pyruvate kinase [PK] | triose-phosphate isomérase | hémolytique non sphérocytaire (héréditaire), type II

WORLD HEALTH ORGANIZATION ICD-10: D55.2

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

Others have searched : andersen disease andersen's disease bückler's type ii corneal dystrophy fazio-londe fehr's spotted corneal dystrophy forbes glycogenosis gsd iv gsd-ii gierke's disease groenouw type ii corneal dystrophy kugelberg-welander najjar-andersen syndrome pompe disease progressive bulbar palsy of childhood spinal muscular atrophy adult form acid maltase deficiency amylopectinosis amylopectinosis brancher deficiency brancher deficiency brancher enzyme deficiency childhood form type ii deficiency distal familia glycogen storage disease glycogen storage disease type ii glycogen storage disease type iv glycogenosis glycogenosis iv glycogenosis type ii hepatorenal glycogenosis hexokinase deficiency juvenile form type iii macular corneal dystrophy macular dystrophy pyruvate kinase scapuloperoneal form touch type triose-phosphate isomerase deficiency type 1 glycogenosis type i glycogen storage disease type at speed type quickly typing at speed von gierke's disease Glycogenosis type II

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'Glycogenosis type II'

Date index:2022-04-25 -

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Translation of "Glycogenosis type II " (English → French) :

Pour agences de traduction et traducteurs - For translation agencies & translators Paris - Brussels - Montreal - Genève - Luxembourg - Madrid Wordscope - Professional computer-assisted translation tools (CAT tools)

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