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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

Traduction de «lipid storage disease » (Anglais → Français) :



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.-+)


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 ]


Other lipid storage disorders

Autres anomalies du stockage des lipides


Disorders of sphingolipid metabolism and other lipid storage disorders

Anomalies du métabolisme des sphingolipides et autres anomalies du stockage des lipides


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


lysosomal disease | lysosomal storage disease

déficit du stockage lysosomal | maladie lysosomiale


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




tubular androblastoma with lipid storage

androblastome tubulaire à cellules lipidiques




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Date index: 2021-01-23
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