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Gierke's disease
Glycogen storage disease I
Hepatorenal glycogenosis
Lipid storage disease
Lipid storage disorders
Lysosomal disease
Lysosomal storage disease
Myopathy in glycogen storage disease
Other lipid storage disorders
Storage disease
Tubular androblastoma with lipid storage
Type 1 glycogenosis
Type I glycogen storage disease
Von Gierke's disease

Translation of "Lipid storage disease " (English → French) :

Lipid storage disease

maladie de surchage lipidique
SNOMEDCT-BE (disorder) / 10741005
SNOMEDCT-BE (disorder) / 10741005


Myopathy in:glycogen storage disease (E74.0+) | lipid storage disorders (E75.-+)

Myopathie au cours d'anomalies de stockage (du) (des):glycogène (E74.0+) | lipides (E75.-+)
WORLD HEALTH ORGANIZATION ICD-10: G73.6*
WORLD HEALTH ORGANIZATION ICD-10: G73.6*


type I glycogen storage disease [ von Gierke's disease | Gierke's disease | type 1 glycogenosis | glycogen storage disease I | hepatorenal glycogenosis ]

maladie de von Gierke [ glycogénose de type I | glycogénose hépato-rénale ]
Liver and Biliary Ducts | Human Diseases - Various
Foie et voies biliaires | Maladies humaines diverses


Other lipid storage disorders

Autres anomalies du stockage des lipides
WORLD HEALTH ORGANIZATION ICD-10: E75.5
WORLD HEALTH ORGANIZATION ICD-10: E75.5


Disorders of sphingolipid metabolism and other lipid storage disorders

Anomalies du métabolisme des sphingolipides et autres anomalies du stockage des lipides
WORLD HEALTH ORGANIZATION ICD-10: E75
WORLD HEALTH ORGANIZATION ICD-10: E75


An extremely rare genetic glycogen storage disease reported in one patient to date. Clinical signs included muscle weakness, cardiac arrhythmia associated with accumulation of abnormal storage material in the heart and glycogen depletion in skeletal

glycogénose avec cardiomyopathie sévère par déficit en glycogénine
SNOMEDCT-BE (disorder) / 717821004
SNOMEDCT-BE (disorder) / 717821004


lysosomal disease | lysosomal storage disease

déficit du stockage lysosomal | maladie lysosomiale
IATE - Health
IATE - Health


A lysosomal storage disease with clinical characteristics of psychomotor retardation and visual abnormalities including corneal clouding, retinal degeneration or strabismus. The disease is rare in the general population but is more prevalent among As

mucolipidose type IV
SNOMEDCT-BE (disorder) / 725296006
SNOMEDCT-BE (disorder) / 725296006


storage disease

maladie de conservation
Plant Diseases | Crop Storage Facilities
Maladies des plantes | Entreposage des récoltes


tubular androblastoma with lipid storage

androblastome tubulaire à cellules lipidiques
The Genitals
Organes génitaux




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'Lipid storage disease'

Date index:2021-05-13 -

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