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Amylopectinosis
Amylopectinosis brancher deficiency
Andersen disease
Andersen's disease
Brancher deficiency
Brancher enzyme deficiency
Drug-induced enzyme deficiency anaemia
Enzyme deficiency
Familia
GSD IV
Glycogen storage disease type IV
Glycogenosis IV
HMP
Najjar-Andersen syndrome
Shunt pathway

Übersetzung für "brancher enzyme deficiency " (Englisch → Französisch) :

brancher enzyme deficiency [ amylopectinosis ]
http://www.btb.termiumplus.gc. (...) (...) [HTML] [2018-01-01]
déficience en enzyme branchante
http://www.btb.termiumplus.gc. (...) (...) [HTML] [2018-01-01]
http://www.btb.termiumplus.gc. (...) [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]
enzyme deficiency
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
déficience enzymatique
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
http://iate.europa.eu/FindTerm (...) [HTML] [2017-12-31]
combined immunodeficiency secondary to ADA enzyme deficiency
http://www.btb.termiumplus.gc. (...) (...) [HTML] [2018-01-01]
déficit immunitaire combiné sévère associé à un déficit en adénosine désaminase
http://www.btb.termiumplus.gc. (...) (...) [HTML] [2018-01-01]
http://www.btb.termiumplus.gc. (...) [HTML] [2018-01-01]
Anaemia (due to):enzyme deficiencies, except G6PD, related to the hexose monophosphate [HMP] shunt pathway | haemolytic nonspherocytic (hereditary), type I
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
Anémie (due à):déficit enzymatique, excepté G6PD, de la voie de l'hexose monophosphate [HMP] | hémolytique non sphérocytaire (héréditaire), type I
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
https://icd.who.int/browse10/2 (...) [HTML] [2018-01-01]
Congenital adrenogenital disorders associated with enzyme deficiency
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
Anomalies génito-surrénaliennes congénitales liées à un déficit enzymatique
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
https://icd.who.int/browse10/2 (...) [HTML] [2018-01-01]
Drug-induced enzyme deficiency anaemia
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
Anémie par déficit enzymatique, due à des médicaments
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
https://icd.who.int/browse10/2 (...) [HTML] [2018-01-01]


Andere haben gesucht : andersen disease     andersen's disease     drug-induced enzyme deficiency anaemia     gsd iv     najjar-andersen syndrome     amylopectinosis     amylopectinosis brancher deficiency     brancher deficiency     brancher enzyme deficiency     enzyme deficiency     familia     glycogen storage disease type iv     glycogenosis iv     haemolytic nonspherocytic type     shunt pathway     


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Date index: 2022-07-29
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