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Translation of "unilateral " (English → French) :
TERMINOLOGY
see also In-Context Translations below unilateral | one-sided
unilatéral | qui n'affecte qu'un côté (du corps ou d'un organe)
UGENT - Medical terms -
UGENT - Medical terms -
A rare developmental defect during embryogenesis syndrome, with characteristics of normal female karyotype, normal ovaries, male or ambiguous genitalia, urinary tract malformations (ranging from bilateral renal agenesis to mild unilateral hydronephro
syndrome d'anomalie du développement sexuel 46,XX-anomalies anorectales
SNOMEDCT-BE (ranging from bilateral renal agenesis to mild unilateral hydronephro / 733622000
SNOMEDCT-BE (disorder) / 733622000
A rare genetic cranial malformation with characteristics of unilateral or bilateral synostosis of the lambdoid suture in multiple members of a single family. Unilateral cases typically present ipsilateral occipitomastoid bulge, compensatory contralat
synostose lambdoïde familiale
SNOMEDCT-BE (disorder) / 766884000
SNOMEDCT-BE (disorder) / 766884000
A rare otorhinolaryngologic disease with characteristics of the unilateral or bilateral dehiscence of the bone(s) overlying the superior (most common), lateral or posterior semicircular canal(s). Patients present audiological (autophony, aural fullne
syndrome de déhiscence du canal semi-circulaire
SNOMEDCT-BE (s) overlying the superior (most common), lateral or posterior semicircular canal(s). Patients present audiological (autophony, aural fullne / 768933005
SNOMEDCT-BE (disorder) / 768933005
A rare developmental defect during embryogenesis with characteristics of ventral, unilateral or bilateral protrusion of extraperitoneal fat, peritoneum and/or intra-abdominal organs through a defect in the spigelian fascia (spigelian hernia), associa
syndrome de cryptorchidie-hernie de Spiegel
SNOMEDCT-BE (spigelian hernia), associa / 773623000
SNOMEDCT-BE (disorder) / 773623000
A rare malignant, epithelial ovarian neoplasm, composed of clear, eosinophilic and hobnail cells displaying variable degrees of tubulocystic, papillary and solid histological patterns, macroscopically appearing as a typically unilateral mass in the o
adénocarcinome à cellules claires de l'ovaire
SNOMEDCT-BE (disorder) / 763131005
SNOMEDCT-BE (disorder) / 763131005
A rare epilepsy syndrome defined by seizures originating in limbic areas of the mesial temporal lobe, particularly in the hippocampus, amygdala, and in the parahippocampal gyrus and its connections, and hippocampal sclerosis, usually unilateral or as
epilepsie du lobe mésio-temporal avec sclérose de l'hippocampe
SNOMEDCT-BE (disorder) / 770643005
SNOMEDCT-BE (disorder) / 770643005
A surgically correctable form of primary hyperaldosteronism characterised by renin suppression, unilateral aldosterone hypersecretion, and moderate to severe hypertension secondary to hyperplasia of the adrenal gland. May be associated with hypokalae
hyperplasie surrénalienne unilatérale primitive
SNOMEDCT-BE (disorder) / 715868005
SNOMEDCT-BE (disorder) / 715868005
A rare indolent subtype of clear cell renal carcinoma arising from epithelial cells in the renal cortex. It most frequently manifests with a well-circumscribed, well-encapsulated, unicentric, unilateral, small tumor that typically does not metastasiz
carcinome rénal papillaire à cellules claires
SNOMEDCT-BE (disorder) / 734015000
SNOMEDCT-BE (disorder) / 734015000
An extremely rare neurological disorder presumed to result from maldevelopment of the facial nucleus and/or cranial nerve reported in fewer than 10 families to date. It manifests as non-progressive, isolated, unilateral or bilateral, symmetrical or a
paralysie faciale congénitale héréditaire isolée
SNOMEDCT-BE (disorder) / 733091002
SNOMEDCT-BE (disorder) / 733091002
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'unilateral'
Date index:2022-12-10 -
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