Category:Glycogen storage disease type II

**glycogen storage disease II**
	human disease
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Instance of	rare disease; class of disease;
Subclass of	glycogen storage disease; hypertrophic cardiomyopathy; muscular glycogenosis; lysosomal disease with restrictive cardiomyopathy; lysosomal disease with hypertrophic cardiomyopathy; glycogen storage disease with hypertrophic cardiomyopathy; lysosomal glycogen storage disease; disease;
Named after	Johannes C. Pompe;
Authority file
	Q1365789; NL CR AUT ID: ph944185; National Library of Israel J9U ID: 987007556595605171
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<nowiki>malattia di Pompe; maladie de Pompe; Помпеова болест; 庞贝氏症; داء اختزان الغلايكوجين النمط الثاني; Penyakit Pompe; 龐貝氏症; Morbus Pompe; doença de Pompe; Enfermedad de Pompe; گلیکوژنوز نوع دو; 龐貝氏症; Pompeova bolest; malaltia de Pompe; ポンペ病; Болезнь Помпе; glycogeenstapelingsziekte type II; Penyakit Pompe; Choroba Pompego; Захворювання Помпе; Pompe xəstəliyi; 龐貝氏症; מחלת אגירת גליקוגן מסוג 2; glykogeninlagringssjukdom typ II; Pompen tauti; glycogen storage disease II; malsano de Pompe; Pompeho choroba; Bolest skladištenja glikogena tipa II; malattia neuromuscolare rara, caratterizzata da un difetto del metabolismo del glicogeno il quale si accumula in modo anomalo nei tessuti,; maladie génétique progressive et souvent fatale en rapport avec une anomalie de fonctionnement de l'alpha-1,4-glucosidase acide, une enzyme lysosomiale qui hydrolyse le glycogène en glucose; хвороба людини; редкое наследственное заболевание с аутосомно-рецессивным механизмом наследования, связанное с повреждением мышечных и нервных клеток по всему организму; Krankheit; krooninen neuromuskulaarinen sairaus; human disease; نوعی ناهنجاری متابولیک مادرزادی; մարդու հիվանդություն; Glicogenosi di tipo 2; Morbo di Pompe; 糖原病II型; 酸性マルターゼ欠損症; glycogénose type 2; Glykogen lagringssjukdom typ II; GSD II; Glikogenoza typu II; מחלת פומפה; morbus Pompe; zure-maltasedeficiëntie; ziekte van Pompe; Penyakit Penyimpanan Glikogen; Saure Maltasemangel; Pompesche Krankheit; Pompe-Krankheit; Glucogenosis tipo II; Pompe disease; acid maltase deficiency; Generalized glycogenosis (disorder); Glycogen storage disease, type II (disorder); Glycogenosis, type 2; Lysosomal alpha-1,4-glucosidase deficiency (disorder); Pompe's disease; deficiency of glucoamylase; deficiency of maltase; glycogen storage disease type II; Lysosomal alpha-1,4-glucosidase deficiency; Glycogen storage disease, type II; Generalized glycogenosis; Glycogen storage disease type 2; Alpha-1,4-glucosidase acid deficiency; GLYCOGEN STORAGE DISEASE II; Gsd 2; Glycogenosis type 2; Gaa Deficiency; Cardiomegalia Glycogenica Diffusa; GSD2; GSD type II; GSD due to acid maltase deficiency; GSD type 2; Glycogenosis type II; Glycogenosis due to acid maltase deficiency; Alpha-1,4-Glucosidase Deficiency; GLYCOGEN STORAGE DISEASE II; GSD2; Glycogen storage disease due to acid maltase deficiency; Glycogenosis, Generalized, Cardiac Form; بیماری پومپه; Pompeho nemoc; Deficit kyselé maltázy; Pompeova choroba; Glykogenóza typu II; Morbus Pompe; Pompeova nemoc; POMPE</nowiki>