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Addison-Schilder
Adrenoleukodystrophy
Amylopectinosis
Amylopectinosis brancher deficiency
Andersen disease
Andersen's disease
Brancher deficiency
Brancher enzyme deficiency
Carnitin
Carnitine
Carnitine deficiency
Carnitine palmitoyltransferase II deficiency
Deficiency
Familia
GSD IV
Glycogen storage disease type IV
Glycogenosis IV
Hexokinase deficiency
Muscle carnitine palmityltransferase deficiency
Najjar-Andersen syndrome
PK
Pyruvate kinase
Sulfur deficient
Sulfur-deficient
Sulphur deficient
Sulphur-deficient
Triose-phosphate isomerase deficiency

Translation of "Carnitine deficiency " (English → French) :

carnitine deficiency
http://www.btb.termiumplus.gc. (...) (...) [HTML] [2018-01-01]
déficience en carnitine
Animal Husbandry
Élevage des animaux
http://www.btb.termiumplus.gc. (...) (...) [HTML] [2018-01-01]
http://www.btb.termiumplus.gc. (...) [HTML] [2018-01-01]
Carnitine palmitoyltransferase II deficiency
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
déficit en carnitine palmitoyltransférase II
SNOMEDCT-BE (disorder) / 238002005
SNOMEDCT-BE (disorder) / 238002005
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]
Adrenoleukodystrophy [Addison-Schilder] Muscle carnitine palmityltransferase deficiency
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
Adrénoleucodystrophie [Addison-Schilder] Carence en carnitine palmityltransférase musculaire
WORLD HEALTH ORGANIZATION ICD-10: E71.3
WORLD HEALTH ORGANIZATION ICD-10: E71.3
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
https://icd.who.int/browse10/2 (...) [HTML] [2018-01-01]
carnitin | carnitine
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
carnitine
IATE - Health | Chemistry
IATE - Health | Chemistry
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
http://iate.europa.eu/FindTerm (...) [HTML] [2017-12-31]
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 ]
Endocrine System and Metabolism | Liver and Biliary Ducts
Systèmes endocrinien et métabolique | Foie et voies biliaires
http://www.btb.termiumplus.gc. (...) (...) [HTML] [2018-01-01]
http://www.btb.termiumplus.gc. (...) [HTML] [2018-01-01]
sulphur deficient [ sulphur-deficient | sulfur-deficient | sulfur deficient ]
http://www.btb.termiumplus.gc. (...) (...) [HTML] [2018-01-01]
déficient en soufre
Geochemistry
Géochimie
http://www.btb.termiumplus.gc. (...) (...) [HTML] [2018-01-01]
http://www.btb.termiumplus.gc. (...) [HTML] [2018-01-01]
Melanocortin 4 receptor (MC4R) deficiency is the commonest form of monogenic obesity identified so far. MC4R deficiency is characterized by severe obesity, an increase in lean body mass and bone mineral density, increased linear growth in early child
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
obésité par déficit du récepteur de la mélanocortine 4
SNOMEDCT-BE (MC4R) deficiency is the commonest form of monogenic obesity identified so far. MC4R deficiency is characterized by severe obesity, an increase in lean body mass and bone mineral density, increased linear growth in early child / 717269008
SNOMEDCT-BE (disorder) / 717269008
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]
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
WORLD HEALTH ORGANIZATION ICD-10: D55.2
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
https://icd.who.int/browse10/2 (...) [HTML] [2018-01-01]
Carnitine
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
Carnitine
SNOMEDCT-CA (substance) / 59888006
SNOMEDCT-CA (substance) / 59888006
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]
Vitamin B12 deficiency anaemia due to intrinsic factor deficiency
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
Anémie par carence en vitamine B12 due à une carence en facteur intrinsèque
WORLD HEALTH ORGANIZATION ICD-10: D51.0
WORLD HEALTH ORGANIZATION ICD-10: D51.0
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
https://icd.who.int/browse10/2 (...) [HTML] [2018-01-01]


Others have searched : addison-schilder    adrenoleukodystrophy    andersen disease    andersen's disease    carnitine    carnitine palmitoyltransferase ii deficiency    gsd iv    muscle carnitine palmityltransferase deficiency    najjar-andersen syndrome    amylopectinosis    amylopectinosis brancher deficiency    brancher deficiency    brancher enzyme deficiency    carnitin    carnitine deficiency    deficiency    familia    glycogen storage disease type iv    glycogenosis iv    hexokinase deficiency    pyruvate kinase    sulfur deficient    sulfur-deficient    sulphur deficient    sulphur-deficient    triose-phosphate isomerase deficiency    Carnitine deficiency    


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'Carnitine deficiency'

Date index:2021-03-04 -

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