Glycogen storage disease due to glucose-6-phosphate system deficiency (Q84780): Difference between revisions

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Latest revision as of 10:08, 15 August 2026

Glycogenosis due to glucose-6-phosphatase (G6P) deficiency or glycogen storage disease, (GSD), type 1, is a group of inherited metabolic diseases, including types a and b (see these terms), and characterised by poor tolerance to fasting, growth retardation and hepatomegaly resulting from accumulation of glycogen and fat in the liver.

Language	Label	Description	Also known as
default for all languages	ID_523888904
English	Glycogen storage disease due to glucose-6-phosphate system deficiency	Glycogenosis due to glucose-6-phosphatase (G6P) deficiency or glycogen storage disease, (GSD), type 1, is a group of inherited metabolic diseases, including types a and b (see these terms), and characterised by poor tolerance to fasting, growth retardation and hepatomegaly resulting from accumulation of glycogen and fat in the liver.