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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 ]
http://www.btb.termiumplus.gc. (...) (...) [HTML] [2018-01-01]
maladie de von Gierke [ glycogénose de type I | glycogénose hépato-rénale ]
http://www.btb.termiumplus.gc. (...) (...) [HTML] [2018-01-01]
http://www.btb.termiumplus.gc. (...) [HTML] [2018-01-01]
hepatorenal syndrome
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
syndrome hépato-rénal
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
http://iate.europa.eu/FindTerm (...) [HTML] [2017-12-31]
glycogen storage disease | glycogenosis | glycogenopathy | dextrinosis | glycogenoses
http://gdt.oqlf.gouv.qc.ca/fic (...) (...) [HTML] [2018-01-01]
glycogénose | thésaurose glycogénique | glycogénoses
http://gdt.oqlf.gouv.qc.ca/fic (...) (...) [HTML] [2018-01-01]
http://gdt.oqlf.gouv.qc.ca/fic (...) [HTML] [2018-01-01]
tyrosinaemia | hereditary tyrosinemia | tyrosinosis | hereditary tyrosinaemia | Baber's syndrome | atypical tyrosinosis | genuine tyrosyluria | hypermethioninaemia | inborn hepatorenal dysfunction
http://gdt.oqlf.gouv.qc.ca/fic (...) (...) [HTML] [2018-01-01]
tyrosinémie | tyrosinémie héréditaire | tyrosinémie de type 1 | tyrosinose héréditaire | tyrosinose congénitale | tyrosinose
http://gdt.oqlf.gouv.qc.ca/fic (...) (...) [HTML] [2018-01-01]
http://gdt.oqlf.gouv.qc.ca/fic (...) [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 ]
http://www.btb.termiumplus.gc. (...) (...) [HTML] [2018-01-01]
http://www.btb.termiumplus.gc. (...) [HTML] [2018-01-01]
glycogen storage disease [ glycogen disease | glycogenosis ]
http://www.btb.termiumplus.gc. (...) (...) [HTML] [2018-01-01]
glycogénose
http://www.btb.termiumplus.gc. (...) (...) [HTML] [2018-01-01]
http://www.btb.termiumplus.gc. (...) [HTML] [2018-01-01]
Forbes glycogenosis
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
maladie de Forbes
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
http://iate.europa.eu/FindTerm (...) [HTML] [2017-12-31]
glycogenosis
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
glycogénose
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
http://iate.europa.eu/FindTerm (...) [HTML] [2017-12-31]
Hepatorenal failure
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
syndrome hépatorénal
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]
Glycogenosis, NOS
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
maladie de stockage du glycogène
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]


D'autres ont cherché : andersen disease     andersen's disease     baber's syndrome     forbes glycogenosis     gsd iv     gierke's disease     glycogenosis nos     hepatorenal failure     najjar-andersen syndrome     amylopectinosis     amylopectinosis brancher deficiency     atypical tyrosinosis     brancher deficiency     brancher enzyme deficiency     dextrinosis     familia     genuine tyrosyluria     glycogen disease     glycogen storage disease     glycogen storage disease type iv     glycogenopathy     glycogenoses     glycogenosis     glycogenosis iv     hepatorenal glycogenosis     hepatorenal syndrome     hereditary tyrosinaemia     hereditary tyrosinemia     hypermethioninaemia     inborn hepatorenal dysfunction     type 1 glycogenosis     type i glycogen storage disease     tyrosinaemia     tyrosinosis     von gierke's disease     


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Date index: 2023-01-30
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