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Translation of "characterized by total " (English → French) :
TERMINOLOGY
see also In-Context Translations below 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
Definition: P
ersonality disorder characterized by a definite tendency to act impulsively and without consideration of the consequences; the mood is unpredictable and capricious. There is a liability to outbursts of emotion and an incapacity to control the behavioural explosions. There is a tendency to quarrelsome behaviour and to conflicts with others, especially when impulsive acts are thwarted or censored. Two types may be distinguished: the impulsive type, characterized predominantly by emotional instability and lack of impulse control, and the borderline type, characterized in addition by disturbances in self-image, aims, and intern
...[+++]al preferences, by chronic feelings of emptiness, by intense and unstable interpersonal relationships, and by a tendency to self-destructive behaviour, including suicide gestures and attempts. | Personality (disorder):aggressive | borderline | explosive
Définition: Trouble
de la personnalité caractérisé par une tendance nette à agir de façon impulsive et sans considération pour les conséquences possibles, une humeur imprévisible et capricieuse, une tendance aux explosions émotionnelles et une difficulté à contrôler les comportements impulsifs, une tendance à adopter un comportement querelleur et à entrer en conflit avec les autres, particulièrement lorsque les actes impulsifs sont contrariés ou empêchés. Deux types peuvent être distingués: le type impulsif, caractérisé principalement par une instabilité émotionnelle et un manque de contrôle des impulsions, et le type borderline, caracté
...[+++]risé en outre par des perturbations de l'image de soi, de l'établissement de projets et des préférences personnelles, par un sentiment chronique de vide intérieur, par des relations interpersonnelles intenses et instables et par une tendance à adopter un comportement auto-destructeur, comprenant des tentatives de suicide et des gestes suicidaires. | Personnalité:agressive | borderline | explosiveWORLD HEALTH ORGANIZATION ICD-10: F60.3
WORLD HEALTH ORGANIZATION ICD-10: F60.3
A very rare genetic disorder of water balance, closely resembling the far more frequent syndrome of inappropriate antidiuretic secretion (SIAD) characterized by hypotonic hyponatremia due to impaired free water excretion and undetectable or low plasm
syndrome néphrogénique d'antidiurèse inappropriée
SNOMEDCT-CA (SIAD) characterized by hypotonic hyponatremia due to impaired free water excretion and undetectable or low plasm / 723440000
SNOMEDCT-CA (trouble) / 723440000
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
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
An extremely rare subtype of autosomal recessive intermediate Charcot-Marie-Tooth (CMT) disease characterized by a CMT neuropathy associated with developmental delay, self-abusive behavior, dysmorphic features and vestibular Schwannoma. Motor nerve c
maladie de Charcot-Marie-Tooth intermédiaire autosomique récessive type B
SNOMEDCT-BE (CMT) disease characterized by a CMT neuropathy associated with developmental delay, self-abusive behavior, dysmorphic features and vestibular Schwannoma. Motor nerve c / 773330000
SNOMEDCT-BE (disorder) / 773330000
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
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
A rare genetic congenital hypothyroidism disorder with characteristics of mild global developmental delay in childhood, short stature, delayed bone age and abnormal thyroid and selenium levels in serum (high total and free T4 concentrations, low T3,
petite taille-retard d'âge osseux par déficit du métabolisme de l'hormone thyroïdienne
SNOMEDCT-BE (high total and free T4 concentrations, low T3, / 763890006
SNOMEDCT-BE (disorder) / 763890006
A rare cardiovascular morphological anomaly due to maldevelopment of embryonal aorta resulting in right aortic arch and left ligamentum arteriosum characterized by tracheoesophageal compression symptoms (stridor, dyspnea, dysphagia, apneic episodes,
anomalie de Neuhauser
SNOMEDCT-BE (stridor, dyspnea, dysphagia, apneic episodes, / 766751007
SNOMEDCT-BE (disorder) / 766751007
A rare chromosomal anomaly syndrome characterized by pre and postnatal growth restriction, developmental delay, variable degrees of intellectual disability, hand and foot anomalies (for example brachy/clinodactyly, talipes equinovarus, nail hypoplasi
monosomie distale 15q
SNOMEDCT-BE (for example brachy/clinodactyly, talipes equinovarus, nail hypoplasi / 766050000
SNOMEDCT-BE (disorder) / 766050000
A rare inborn error of metabolism characterized by persistent hypermethioninemia with increased levels of S-adenosylmethionine and S-adenosylhomocysteine which manifests with encephalopathy, severe global developmental delay, mild to severe liver dys
encéphalopathie associée à une hyperméthioninémie par déficit en adénosine kinase
SNOMEDCT-BE (disorder) / 763721006
SNOMEDCT-BE (disorder) / 763721006
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'characterized by total'
Date index:2022-06-09 -
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