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Biotin
Biotin only product
Biotin-dependent carboxylase deficiency
Cyanocobalamin
Deficiency
Deficiency biotin
Folate
Folic acid
Hexokinase deficiency
PK
Pantothenic acid
Pyruvate kinase
Triose-phosphate isomerase deficiency
Vitamin B12

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

Deficiency:biotin | cyanocobalamin | folate | folic acid | pantothenic acid | vitamin B12
https://icd.who.int/browse10/2 (...) (...) [HTML]
Carence en:acide folique | acide pantothénique | biotine | cyanocobalamine | folate | vitamine B12
WORLD HEALTH ORGANIZATION ICD-10: E53.8
WORLD HEALTH ORGANIZATION ICD-10: E53.8
https://icd.who.int/browse10/2 (...) (...) [HTML]
https://icd.who.int/browse10/2 (...) [HTML]
Biotin-dependent carboxylase deficiency
https://icd.who.int/browse10/2 (...) (...) [HTML]
Déficit en carboxylase biotine-dépendante
WORLD HEALTH ORGANIZATION ICD-10: D81.8
WORLD HEALTH ORGANIZATION ICD-10: D81.8
https://icd.who.int/browse10/2 (...) (...) [HTML]
https://icd.who.int/browse10/2 (...) [HTML]
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
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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
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https://browser.ihtsdotools.or (...) [HTML]
Anaemia:haemolytic nonspherocytic (hereditary), type II | hexokinase deficiency | pyruvate kinase [PK] deficiency | triose-phosphate isomerase deficiency
https://icd.who.int/browse10/2 (...) (...) [HTML]
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]
https://icd.who.int/browse10/2 (...) [HTML]
Biotin
https://browser.ihtsdotools.or (...) (...) [HTML]
produit contenant de la biotine
SNOMEDCT-BE (medicinal product) / 13813003
SNOMEDCT-BE (medicinal product) / 13813003
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]
Biotin only product
https://browser.ihtsdotools.or (...) (...) [HTML]
médicament contenant seulement biotine
SNOMEDCT-CA (produit médicinal) / 774863007
SNOMEDCT-CA (produit médicinal) / 774863007
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]
Disease that is characterized clinically by neonatal hyperpigmentation, hypoglycemia, failure to thrive, and recurrent infections and biochemically by glucocorticoid deficiency without mineralocorticoid deficiency. The disease usually presents in inf
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déficit isolé familial en glucocorticoïdes
SNOMEDCT-BE (disorder) / 765326001
SNOMEDCT-BE (disorder) / 765326001
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https://browser.ihtsdotools.or (...) [HTML]
Congenital multiple pituitary hormone deficiency including somatotroph, thyrotroph, lactotroph, corticotroph or gonadotroph deficiencies, due to mutations of pituitary transcription factors involved in pituitary ontogenesis. Rare when compared with t
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déficits hypohysaires multiples de cause génétique identifée
SNOMEDCT-BE (disorder) / 718182008
SNOMEDCT-BE (disorder) / 718182008
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https://browser.ihtsdotools.or (...) [HTML]
Short stature due to primary acid-labile subunit (ALS) deficiency is characterized by moderate postnatal growth deficit, markedly low circulating levels of insulin-like growth factor 1 (IGF-1) and insulin-like growth factor binding protein 3 (IGFBP-3
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petite taille par déficit primaire en sous-unité acide labile
SNOMEDCT-BE (ALS) deficiency is characterized by moderate postnatal growth deficit, markedly low circulating levels of insulin-like growth factor 1 (IGF-1) and insulin-like growth factor binding protein 3 (IGFBP-3 / 721074002
SNOMEDCT-BE (disorder) / 721074002
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]
CLBP (ClpB homolog, mitochondrial AAA ATPase chaperonin) deficiency
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acidurie 3-méthylglutaconique type 7
SNOMEDCT-BE (ClpB homolog, mitochondrial AAA ATPase chaperonin) deficiency / 764860006
SNOMEDCT-BE (disorder) / 764860006
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]


Others have searched : biotin    biotin only product    biotin-dependent carboxylase deficiency    deficiency biotin    cyanocobalamin    deficiency    folate    folic acid    hexokinase deficiency    pantothenic acid    pyruvate kinase    triose-phosphate isomerase deficiency    vitamin b12    


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'deficiency biotin'

Date index:2023-07-23 -

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