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AMD
Acid maltase deficiency
GSD-II
Glycogen storage disease
Glycogen storage disease
Glycogen storage disease type II
Glycogenosis type II
Iron storage disease
Lipid storage disorders
Lysosomal disease
Lysosomal storage disease
Myopathy in glycogen storage disease
Pompe disease
Storage disease
Wilson's disease

Vertaling van "Iron storage disease " (Engels → Nederlands) :



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

glycogeenstapelingsziekte type 15


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

myopathie bij | glycogeenstapelingsziekten (E74.0) | myopathie bij | vetstapelingsziekten (E75.-)


A genetically inherited anomaly of glycogen metabolism and a form of glycogen storage disease characterized by fasting hypoglycemia. It is an extremely rare disease; about 20 cases have been reported in the literature so far. The disease appears in i

levergebonden glycogeensynthasedeficiëntie


lysosomal disease | lysosomal storage disease

lysosomale stapelingsziekte


acid maltase deficiency | glycogen storage disease type II | glycogenosis type II | Pompe disease | AMD [Abbr.] | GSD-II [Abbr.]

ziekte van Pompe


Renal tubulo-interstitial disorders in:cystinosis (E72.0+) | glycogen storage disease (E74.0+) | Wilson's disease (E83.0+)

tubulo-interstitiële nieraandoeningen bij | cystinose (E72.0) | tubulo-interstitiële nieraandoeningen bij | glycogeenstapelingsziekte (E74.0) | tubulo-interstitiële nieraandoeningen bij | ziekte van Wilson (E83.1)








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'Iron storage disease' ->

Date index: 2023-09-29
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