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Translation of "fatty degeneration " (English → French) :
TERMINOLOGY
see also In-Context Translations below steatosis | fatty degeneration
stéatose | surcharge en lipides des cellules
UGENT - Medical terms -
UGENT - Medical terms -
Degeneration of heart or myocardium:fatty | senile | Myocardial disease
Dégénérescence du cœur ou du myocarde:graisseuse | sénile | Maladie du myocarde
WORLD HEALTH ORGANIZATION ICD-10: I51.5
WORLD HEALTH ORGANIZATION ICD-10: I51.5
A rare genetic endocrine disease characterized by neonatal macrosomia, asymmetrical overgrowth (typically manifesting as left-sided hemihypertrophy) and recurrent, severe hypoinsulinemic (or hypo ketotic hypo-fatty-acidemic) hypoglycemia in infancy,
hypoglycémie hypoinsulinémique avec hémihypertrophie du corps
SNOMEDCT-BE (typically manifesting as left-sided hemihypertrophy) and recurrent, severe hypoinsulinemic (or hypo ketotic hypo-fatty-acidemic) hypoglycemia in infancy, / 773666007
SNOMEDCT-BE (disorder) / 773666007
Spinocerebellar ataxia type 28 (SCA28) is very rare with main features of juvenile onset and slowly progressive cerebellar ataxia due to Purkinje cell degeneration. The mean age of symptom onset was 19.5 years in the original kindred. Some patients s
ataxie spinocérébelleuse type 28
SNOMEDCT-BE (SCA28) is very rare with main features of juvenile onset and slowly progressive cerebellar ataxia due to Purkinje cell degeneration. The mean age of symptom onset was 19.5 years in the original kindred. Some patients s / 715824008
SNOMEDCT-BE (disorder) / 715824008
A rare hereditary motor and sensory neuropathy with characteristics of intermediate motor median nerve conduction velocities (usually between 25 and 45 m/s) and signs of both axonal degeneration and demyelination without onion bulbs in nerve biopsies
maladie de Charcot-Marie-Tooth intermédiaire autosomique dominante D
SNOMEDCT-BE (usually between 25 and 45 m/s) and signs of both axonal degeneration and demyelination without onion bulbs in nerve biopsies / 765747004
SNOMEDCT-BE (disorder) / 765747004
A rare hereditary motor and sensory neuropathy with characteristics of intermediate motor median nerve conduction velocities (usually between 25 and 45 m/s) and signs of both demyelination and axonal degeneration in nerve biopsies. It presents with m
maladie de Charcot-Marie-Tooth intermédiaire autosomique dominante B
SNOMEDCT-BE (usually between 25 and 45 m/s) and signs of both demyelination and axonal degeneration in nerve biopsies. It presents with m / 765745007
SNOMEDCT-BE (disorder) / 765745007
A rare hereditary motor and sensory neuropathy characterized by intermediate motor median nerve conduction velocities (usually between 25 and 45 m/s) and signs of both demyelination and axonal degeneration in nerve biopsies. It presents with usual cl
maladie de Charcot-Marie-Tooth intermédiaire autosomique dominante A
SNOMEDCT-BE (usually between 25 and 45 m/s) and signs of both demyelination and axonal degeneration in nerve biopsies. It presents with usual cl / 765744006
SNOMEDCT-BE (disorder) / 765744006
Angioid streaks | Cyst | Drusen (degenerative) | Hole | Puckering | of macula | Kuhnt-Junius degeneration Senile macular degeneration (atrophic)(exudative) Toxic maculopathy
Dégénérescence (de):Junius-Kuhnt | maculaire sénile (atrophique) (exsudative) | Druses (dégénératives) | Kyste | Plis | Stries angioïdes | Trou | de la macula | Maculopathie toxique
WORLD HEALTH ORGANIZATION ICD-10: H35.3
WORLD HEALTH ORGANIZATION ICD-10: H35.3
Alcoholic:cerebellar:ataxia | degeneration | cerebral degeneration | encephalopathy | Dysfunction of autonomic nervous system due to alcohol
Ataxie cérébelleuse | Dégénérescence cérébelleuse | Dégénérescence cérébrale | Dysautonomie | Encéphalopathie | alcoolique
WORLD HEALTH ORGANIZATION ICD-10: G31.2
WORLD HEALTH ORGANIZATION ICD-10: G31.2
Dystrophy of fatty tissue
lipodystrophie
SNOMEDCT-BE (disorder) / 71325002
SNOMEDCT-BE (disorder) / 71325002
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'fatty degeneration'
Date index:2023-06-27 -
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