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Translation of "disease small " (English → French) :
TERMINOLOGY
see also In-Context Translations below This syndrome has characteristics of severe short stature with disproportionately short legs, small hands, clinodactyly, valvular heart disease and dysmorphism (ptosis, high-arched palate, abnormal dentition). It has been described in a mother and tw
syndrome de petite taille-valvulopathie cardiaque-dysmorphie
SNOMEDCT-BE (ptosis, high-arched palate, abnormal dentition). It has been described in a mother and tw / 716193004
SNOMEDCT-BE (disorder) / 716193004
A very rare syndrome described in three siblings of one Japanese family with main features of congenital heart disease, round face with depressed nasal bridge, small mouth, short stature, and relatively dark skin and typical dermatoglyphic anomalies,
syndrome de cardiopathie congénitale-face ronde-petite taille
SNOMEDCT-BE (disorder) / 715987000
SNOMEDCT-BE (disorder) / 715987000
An extremely rare subtype of renal cell carcinoma most frequently characterized by a small, solitary, well-circumscribed, unencapsulated renal tumor composed of multiple small to medium-sized cysts with a white or gray, spongy (bubble wrap-like ) cut
carcinome rénal tubulokystique
SNOMEDCT-BE (bubble wrap-like") cut / 733603009
SNOMEDCT-BE (disorder) / 733603009
This syndrome has characteristics of X-linked intellectual deficit and mild variable manifestations, including short stature, small head circumference, sloping forehead, hearing loss, abnormally shaped ears, and small testes. It has been described in
déficience intellectuelle liée à l'X type Abidi
SNOMEDCT-BE (disorder) / 719018008
SNOMEDCT-BE (disorder) / 719018008
Care given to improve the quality of life of patients who have a serious or life-threatening disease. The goal of symptom management is to prevent or treat as early as possible the symptoms of a disease, side effects caused by treatment of a disease,
gestion des symptômes
SNOMEDCT-BE (procedure) / 713148004
SNOMEDCT-BE (procedure) / 713148004
Disease with characteristics of the adult-onset (average age 40 years) of truncal ataxia, gait disturbance and gaze-evoked nystagmus. The disease is slowly progressive with dysarthria and limb ataxia following. Additional manifestations include diplo
ataxie spinocérébelleuse type 38
SNOMEDCT-BE (average age 40 years) of truncal ataxia, gait disturbance and gaze-evoked nystagmus. The disease is slowly progressive with dysarthria and limb ataxia following. Additional manifestations include diplo / 734021001
SNOMEDCT-BE (disorder) / 734021001
Small bowel
intestin grêle
SNOMEDCT-BE (body structure) / 30315005
SNOMEDCT-BE (body structure) / 30315005
A rare form of porokeratosis occurring mainly in adolescence and characterised by small pruritic or painful keratotic papules that first appear on the palms and soles, and may gradually become generalised. The prevalence is unknown but it is one of t
porokératose palmoplantaire et disséminée
SNOMEDCT-BE (disorder) / 718218005
SNOMEDCT-BE (disorder) / 718218005
A rare intestinal disorder of neonates of unknown aetiology. Patients are born with a short small bowel (less than 75 cm in length) that compromises proper intestinal absorption and leads chronic diarrhoea, vomiting and failure to thrive.
syndrome du grêle court congénital
SNOMEDCT-BE (less than 75 cm in length) that compromises proper intestinal absorption and leads chronic diarrhoea, vomiting and failure to thrive. / 715201005
SNOMEDCT-BE (disorder) / 715201005
Small bowel obstruction
obstruction de l'intestin grêle
SNOMEDCT-BE (disorder) / 281255004
SNOMEDCT-BE (disorder) / 281255004
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'disease small'
Date index:2023-12-08 -
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