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AMD
Acid maltase deficiency
Amylopectinosis
Amylopectinosis brancher deficiency
Andersen disease
Andersen's disease
Brancher deficiency
Brancher enzyme deficiency
Cardiac glycogenosis Disease Andersen
Cori
Familia
Forbes
Forbes glycogenosis
GSD IV
GSD-II
Gierke's disease
Glycogen storage disease I
Glycogen storage disease type II
Glycogen storage disease type IV
Glycogenosis
Glycogenosis IV
Glycogenosis type II
Hepatorenal glycogenosis
Hers
Liver phosphorylase deficiency
McArdle
Najjar-Andersen syndrome
PIG - Pulmonary interstitial glycogenosis
Pompe
Pompe disease
Tarui
Tauri
Type 1 IFN
Type 1 glycogenosis
Type 1 interferon
Type I glycogen storage disease
Type-1 IFN
Type-1 interferon
Von Gierke
Von Gierke's disease

Translation of "Type 1 glycogenosis " (English → French) :

acid maltase deficiency | glycogen storage disease type II | glycogenosis type II | Pompe disease | AMD [Abbr.] | GSD-II [Abbr.]

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


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

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


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 ]

maladie d'Andersen [ glycogénose musculaire type IV ]
Endocrine System and Metabolism | Liver and Biliary Ducts
Systèmes endocrinien et métabolique | Foie et voies biliaires




Forbes glycogenosis

maladie de Forbes
IATE - Health
IATE - Health


PIG - Pulmonary interstitial glycogenosis

glycogénose interstitielle pulmonaire
SNOMEDCT-BE (disorder) / 707551007
SNOMEDCT-BE (disorder) / 707551007


Cardiac glycogenosis Disease:Andersen | Cori | Forbes | Hers | McArdle | Pompe | Tarui | Tauri | von Gierke | Liver phosphorylase deficiency

Déficit en phosphorylase hépatique Glycogénose cardiaque Maladie de:Andersen | Cori | Forbes | Hers | McArdle | Pompe | Tauri | von Gierke
WORLD HEALTH ORGANIZATION ICD-10: E74.0
WORLD HEALTH ORGANIZATION ICD-10: E74.0


Glycogenosis, NOS

maladie de stockage du glycogène
SNOMEDCT-BE (disorder) / 29633007
SNOMEDCT-BE (disorder) / 29633007


A group of tyrosine related oculocutaneous albinism (OCA1) that includes OCA1A, OCA1B, type 1 minimal pigment oculocutaneous albinism (OCA1-MP) and type 1 temperature sensitive oculocutaneous albinism (OCA1-TS). The phenotypic spectrum seen in OCA1 i

albinisme oculo-cutané type 1
SNOMEDCT-BE (OCA1) that includes OCA1A, OCA1B, type 1 minimal pigment oculocutaneous albinism (OCA1-MP) and type 1 temperature sensitive oculocutaneous albinism (OCA1-TS). The phenotypic spectrum seen in OCA1 i / 765146000
SNOMEDCT-BE (disorder) / 765146000


type 1 interferon [ type-1 interferon | type 1 IFN | type-1 IFN ]

interféron de type 1 [ IFN de type 1 ]
Immunology
Immunologie




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'Type 1 glycogenosis'

Date index:2021-12-16 -

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