Glycogen storage disease due to muscle glycogen phosphorylase kinase deficiency (Q100848): Difference between revisions
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| description / pt-br | description / pt-br | ||
A doença de depósito de glicogênio devido à deficiência de fosforilase quinase muscular é um erro inato benigno do metabolismo do glicogênio caracterizado pela intolerância ao exercício. | |||
| description / en | description / en | ||
Glycogen storage disease due to muscle phosphorylase kinase (PhK) deficiency is a benign inborn error of glycogen metabolism characterised by exercise intolerance. | |||
Revision as of 17:37, 16 August 2026
Glycogen storage disease due to muscle phosphorylase kinase (PhK) deficiency is a benign inborn error of glycogen metabolism characterised by exercise intolerance.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_273845529 |
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| English | Glycogen storage disease due to muscle glycogen phosphorylase kinase deficiency |
Glycogen storage disease due to muscle phosphorylase kinase (PhK) deficiency is a benign inborn error of glycogen metabolism characterised by exercise intolerance. |
