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Acquired iodine-deficiency hypothyroidism NOS
Borderline hypothyroidism
Hypothyroid
Hypothyroid adiposity
Hypothyroidism
Underactive thyroid

Translation of "Hypothyroidism NOS " (English → French) :

TERMINOLOGY
see also In-Context Translations below
hypothyroid adiposity

obésité thyroïdienne
IATE - Health
IATE - Health


hypothyroid

hypothyroïdien | hypothyroïdienne
IATE - Health
IATE - Health


hypothyroidism | underactive thyroid

hypothyroïdie | hypothyroïdisme
IATE - Health
IATE - Health


Congenital iodine-deficiency hypothyroidism NOS Endemic cretinism NOS

Crétinisme endémique SAI Hypothyroïdie par insuffisance congénitale en iode SAI
WORLD HEALTH ORGANIZATION ICD-10: E00.9
WORLD HEALTH ORGANIZATION ICD-10: E00.9


Idiopathic congenital hypothyroidism is a type of primary congenital hypothyroidism whose cause and prevalence are unknown. Clinical manifestations are those of other forms of congenital hypothyroidism. Goiter is always absent. Ultrasound examination

hypothyroïdie congénitale idiopathique
SNOMEDCT-BE (disorder) / 717334008
SNOMEDCT-BE (disorder) / 717334008


endemic conditions associated with environmental iodine deficiency either directly or as a consequence of maternal iodine deficiency. Some of the conditions have no current hypothyroidism but are the consequence of inadequate thyroid hormone secretion in the developing fetus. Environmental goitrogens may be associated.

maladies endémiques dues à une insuffisance en iode de l'environnement soit directe, soit résultant d'une insuffisance thyroïdienne maternelle. Certaines de ces maladies ne correspondent pas à une hypothyroïdie en cours mais sont la conséquence d'une sécrétion anormale de l'hormone thyroïdienne au cours du développement du fœtus. Le goitre endémique peut y être associé.
WORLD HEALTH ORGANIZATION ICD-10: E00
WORLD HEALTH ORGANIZATION ICD-10: E00


Acquired iodine-deficiency hypothyroidism NOS

Hypothyroïdie par carence acquise en iode SAI
WORLD HEALTH ORGANIZATION ICD-10: E01.8
WORLD HEALTH ORGANIZATION ICD-10: E01.8


Syndrome that is characterized by total color blindness caused by progressive cone dystrophy, degenerative liver disease, and endocrine dysfunction (hypothyroidism, diabetes, repeated abortions or infertility). It has been described in six females fr

syndrome rétino-hépato-endocrinologique
SNOMEDCT-BE (hypothyroidism, diabetes, repeated abortions or infertility). It has been described in six females fr / 724000006
SNOMEDCT-BE (disorder) / 724000006


Descriptive study of the results of the congenital hypothyroidism screening program of three Quebec municipalities and the relationship to chlorine dioxide use in drinking water (1993-1998)

Étude descriptive des résultats du programme de dépistage de l'hypothyroïdie congénitale de trois municipalités québécoises en fonction de l'utilisation du dioxyde de chlore comme désinfectant de l'eau potable (1993-1998)
Titles of Monographs | The Thyroid | Environment
Titres de monographies | Thyroïde | Environnement


Borderline hypothyroidism

hypothyroïdie subclinique
SNOMEDCT-BE (disorder) / 54823002
SNOMEDCT-BE (disorder) / 54823002
IN-CONTEXT TRANSLATIONS
Neonatal screening for Phenylketonuria and congenital hypothyroidism is current practice in Europe and proved highly efficient in preventing disabilities in affected children.

Le dépistage de la phénylcétonurie et de l’hypothyroïdie congénitale chez les nouveau-nés est couramment pratiqué en Europe et s’est révélé très efficace pour prévenir les handicaps chez les enfants atteints.




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'Hypothyroidism NOS'

Date index:2023-08-25 -

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