Glycogen storage disease due to glucose-6-phosphate system deficiency (Q84780): Difference between revisions
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| description / pt-br | description / pt-br | ||
A glicogenose causada por deficiência da glicose-6-fosfatase (G6P) ou doença de depósito do glicogênio tipo 1, é um grupo de doenças metabólicas hereditárias, incluindo os tipos a e b (ver estes termos), e caracterizada por baixa tolerância ao jejum, atraso do crescimento e hepatomegalia resultantes do acúmulo de glicogênio e de gordura no fígado. | |||
| description / en | description / en | ||
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. | |||
Revision as of 10:07, 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 |
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| 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. |
