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Amylopectinosis
Amylopectinosis brancher deficiency
Andersen disease
Andersen's disease
Atypical tyrosinosis
Baber's syndrome
Brancher deficiency
Brancher enzyme deficiency
Dextrinosis
Familia
Forbes glycogenosis
GSD IV
Genuine tyrosyluria
Gierke's disease
Glycogen disease
Glycogen storage disease
Glycogen storage disease I
Glycogen storage disease type IV
Glycogenopathy
Glycogenoses
Glycogenosis
Glycogenosis IV
Hepatorenal failure
Hepatorenal glycogenosis
Hepatorenal syndrome
Hereditary tyrosinaemia
Hereditary tyrosinemia
Hypermethioninaemia
Inborn hepatorenal dysfunction
Najjar-Andersen syndrome
Type 1 glycogenosis
Type I glycogen storage disease
Tyrosinaemia
Tyrosinosis
Von Gierke's disease

Traduction de «hepatorenal glycogenosis » (Anglais → Français) :

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 ]




glycogen storage disease | glycogenosis | glycogenopathy | dextrinosis | glycogenoses

glycogénose | thésaurose glycogénique | glycogénoses


tyrosinaemia | hereditary tyrosinemia | tyrosinosis | hereditary tyrosinaemia | Baber's syndrome | atypical tyrosinosis | genuine tyrosyluria | hypermethioninaemia | inborn hepatorenal dysfunction

tyrosinémie | tyrosinémie héréditaire | tyrosinémie de type 1 | tyrosinose héréditaire | tyrosinose congénitale | tyrosinose


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 ]


glycogen storage disease [ glycogen disease | glycogenosis ]

glycogénose










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