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Translation of "disease lesion " (English → French) :
TERMINOLOGY
see also In-Context Translations below A rare medullar disease defined as a development of a fluid-filled cavity or syrinx within the spinal cord due to blockage of cerebrospinal fluid circulation (for example due to basal arachnoiditis, meningeal carcinomatosis, various mass lesions), sp
syringomyélie secondaire
SNOMEDCT-BE (for example due to basal arachnoiditis, meningeal carcinomatosis, various mass lesions), sp / 770683002
SNOMEDCT-BE (disorder) / 770683002
A rare genetic skin disease characterized by multiple milium-like, comedone-like lesions and skin-colored to hyperpigmented, 1 to 2 mm-sized papules, associated with hypotrichosis and palmar/plantar pits. Lesions are usually first noticed on cheeks o
syndrome d'hamartome basaloïde folliculaire généralisé
SNOMEDCT-BE (disorder) / 766928004
SNOMEDCT-BE (disorder) / 766928004
A potentially fatal neurological disease with characteristics of neuropathological lesions principally involving the brainstem, thalamus and putamen. It has been described in 11 members of one family. Onset occurs during early childhood, typically a
encéphalopathie nécrosante aigüe familiale
SNOMEDCT-BE (disorder) / 723359002
SNOMEDCT-BE (disorder) / 723359002
An early-onset chorioretinal dystrophy with characteristics of large atrophic macular and nasal retinal lesions, nystagmus, myopia, poor vision and slow disease progression. It has been described in two large families. Transmission is autosomal domin
atrophie bifocale choriorétinienne progressive
SNOMEDCT-BE (disorder) / 719266007
SNOMEDCT-BE (disorder) / 719266007
A rare variant of cutaneous lichen planus with the presence of hyperpigmented lichenoid lesions in sun-exposed or flexural areas of the body. A rare disease in Europe but it is common in Indian populations and in the Middle East. The overall prevalen
lichen plan pigmentogène
SNOMEDCT-BE (disorder) / 717061002
SNOMEDCT-BE (disorder) / 717061002
A very rare hereditary skin disease with manifestation of irregularly distributed epidermal hyperkeratosis of the palms and soles. Reported in 35 families worldwide to date. The lesions usually start to develop in early adolescence but can also prese
kératodermie palmoplantaire ponctuée type 1
SNOMEDCT-BE (disorder) / 717184007
SNOMEDCT-BE (disorder) / 717184007
A rare neurologic disease characterized by global developmental delay, intellectual disability, multiple ischemic lesions on brain MRI, behavioral abnormalities, dystonia, choreic movements and pyramidal syndrome, facial dysmorphism (hypertelorism, a
syndrome autosomique récessif de leucoencéphalopathie-infarctus cérébraux-rétinite pigmentaire
SNOMEDCT-BE (hypertelorism, a / 771476007
SNOMEDCT-BE (disorder) / 771476007
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
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
lesion | injury
lésion | lésion
UGENT - Medical terms -
UGENT - Medical terms -
www.wordscope.com (v4.0.br.77)
'disease lesion'
Date index:2021-04-11 -
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