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Translation of "disorders " (English → French) :
TERMINOLOGY
see also In-Context Translations below angioneurotic | vein neuron disorder
angioneurotique (oedème-) | angionieurotique (oedème-)
UGENT - Medical terms -
UGENT - Medical terms -
neuropathy | nervous system disorder
neuropathie | affection du système nerveux (central ou périphérique)
UGENT - Medical terms -
UGENT - Medical terms -
nephrotic | kidney disorder-related
néphrotique | relatif à une atteinte rénale dégénérative
UGENT - Medical terms -
UGENT - Medical terms -
dystonia | muscle disorders
dystonie | rigidité anormale des muscles
UGENT - Medical terms -
UGENT - Medical terms -
A rare genetic disorder with characteristics of lymphadenopathy and/or splenomegaly and recurrent infections due to herpes viruses. Prevalence of this disorder is not known. It is extremely rare with four individuals in one family identified to date.
syndrome lymphoprolifératif auto-immun avec infections virales récurrentes
SNOMEDCT-BE (disorder) / 722290008
SNOMEDCT-BE (disorder) / 722290008
A rare functional disorder with recurrent episodes of torticollis posturing of the head (inclination or tilting of the head to one side) in healthy children. The prevalence is unknown and the benign nature of the disorder probably means that it is un
torticolis paroxystique bénin de l'enfant
SNOMEDCT-BE (inclination or tilting of the head to one side) in healthy children. The prevalence is unknown and the benign nature of the disorder probably means that it is un / 719521002
SNOMEDCT-BE (disorder) / 719521002
A movement disorder with manifestation of episodes of involuntary tremor of the chin and lower lip. The disorder has been described in less than 25 families from Europe and the USA, with a slight male preponderance. Onset usually occurs in childhood
géniospasme héréditaire
SNOMEDCT-BE (disorder) / 718103001
SNOMEDCT-BE (disorder) / 718103001
A disorder, which is not a natural consequence or progression of any pre-existing disorder, resulting from a diagnostic procedure or any form of therapy that is not an intended or expected outcome.
complication iatrogène
SNOMEDCT-BE (disorder) / 35688006
SNOMEDCT-BE (disorder) / 35688006
A rare chromosomal anomaly with characteristics of a predominantly neuropsychiatric phenotype with a few dysmorphic features. Speech delay, learning difficulties, attention deficit hyperactivity disorder, bipolar disorder and aggressiveness have been
syndrome de microduplication 7q11.23 distale
SNOMEDCT-BE (disorder) / 773325004
SNOMEDCT-BE (disorder) / 773325004
An exceedingly rare genetic disorder with characteristics of cutaneous pigmentation anomalies, ocular disorders and hearing loss. The syndrome was described in 1990 in two patients from the same Yemenite family. A brother and sister were described as
syndrome de Warburg-Thomsen
SNOMEDCT-BE (disorder) / 721084001
SNOMEDCT-BE (disorder) / 721084001
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'disorders'
Date index:2023-01-13 -
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