Glycogen storage disease due to glucose-6-phosphatase deficiency (Q100832)
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Glycogenosis due to glucose-6-phosphatase deficiency (G6P) type b, or glycogen storage disease (GSD) type 1b, is a type of glycogenosis due to G6P deficiency associating the clinical features of glycogenosis due to G6P deficiency type a to neutropaenia, and neutrophil dysfunction that are responsible for tendency towards infections, relapsing aphthous gingivostomatitis, and inflammatory bowel disease.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_377675277 |
||
| English | Glycogen storage disease due to glucose-6-phosphatase deficiency |
Glycogenosis due to glucose-6-phosphatase deficiency (G6P) type b, or glycogen storage disease (GSD) type 1b, is a type of glycogenosis due to G6P deficiency associating the clinical features of glycogenosis due to G6P deficiency type a to neutropaenia, and neutrophil dysfunction that are responsible for tendency towards infections, relapsing aphthous gingivostomatitis, and inflammatory bowel disease. |
Statements
CID11:ID_377675277
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