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Translation of "Pituitary hormone " (English → French) :
TERMINOLOGY
see also In-Context Translations below Pituitary hormone receptor
récepteur de l'hormone hypophysaire
SNOMEDCT-CA (substance) / 26024007
SNOMEDCT-CA (substance) / 26024007
Fertile eunuch syndrome Hypogonadotropic hypogonadism Idiopathic growth hormone deficiency Isolated deficiency of:gonadotropin | growth hormone | pituitary hormone | Kallmann's syndrome Lorain-Levi short stature Necrosis of pituitary gland (postpartum) Panhypopituitarism Pituitary:cachexia | insufficiency NOS | short stature | Sheehan's syndrome Simmonds' disease
Cachexie hypophysaire Hypogonadisme hypogonadotrophique Insuffisance (de):hormone de croissance idiopathique | isolée en:gonadotrophine | hormone de croissance | hormone hypophysaire | staturale pituitaire SAI | Maladie de Simmonds Nécrose pituitaire (post-partum) Panhypopituitarisme Syndrome de:eunuchoïdisme fertile | Kallmann | Lorain-Lévi | Sheehan
WORLD HEALTH ORGANIZATION ICD-10: E23.0
WORLD HEALTH ORGANIZATION ICD-10: E23.0
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
déficits hypohysaires multiples de cause génétique identifée
SNOMEDCT-BE (disorder) / 718182008
SNOMEDCT-BE (disorder) / 718182008
This syndrome has characteristics of short stature, anterior pituitary hormone deficiency, small sella turcica and a hypoplastic anterior hypophysis associated with pointed cerebellar tonsils. It has been described in three generations of large Frenc
syndrome de petite taille-anomalies hypophysaires et cérébelleuses-selle turcique anormale
SNOMEDCT-BE (disorder) / 721072003
SNOMEDCT-BE (disorder) / 721072003
Anterior pituitary [adenohypophyseal] hormones
Hormones antéhypophysaires [adénohypophysaires]
WORLD HEALTH ORGANIZATION ICD-10: T38.8
WORLD HEALTH ORGANIZATION ICD-10: T38.8
Pituitary thyroid hormone resistance
résistance hypophysaire aux hormones thyroïdiennes
SNOMEDCT-BE (disorder) / 360348000
SNOMEDCT-BE (disorder) / 360348000
Overproduction of pituitary ACTH Pituitary-dependent hyperadrenocorticism
Hypercorticisme hypophyso-dépendant Hypersécrétion hypophysaire d'ACTH
WORLD HEALTH ORGANIZATION ICD-10: E24.0
WORLD HEALTH ORGANIZATION ICD-10: E24.0
hypophyseal | pituitary gland-related
hypophysaire | relatif à l'hypophyse (= glande endocrine)
UGENT - Medical terms -
UGENT - Medical terms -
Primary pigmented nodular adrenocortical disease (PPNAD) is a form of bilateral adrenocortical hyperplasia that is often associated with adrenocorticotrophin hormone independent Cushing syndrome. The disease has characteristics of small to normal siz
dysplasie micronodulaire pigmentée des surrénales
SNOMEDCT-BE (PPNAD) is a form of bilateral adrenocortical hyperplasia that is often associated with adrenocorticotrophin hormone independent Cushing syndrome. The disease has characteristics of small to normal siz / 719274008
SNOMEDCT-BE (disorder) / 719274008
Increased secretion from endocrine pancreas of:growth hormone-releasing hormone | pancreatic polypeptide | somatostatin | vasoactive-intestinal polypeptide
Hypersécrétion du pancréas endocrine de:polypeptide:intestinal vaso-actif | pancréatique | releasing factor de l'hormone de croissance | somatostatine
WORLD HEALTH ORGANIZATION ICD-10: E16.8
WORLD HEALTH ORGANIZATION ICD-10: E16.8
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'Pituitary hormone'
Date index:2024-02-17 -
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