glycogen storage disease IXd (Q32146382)
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glycogen storage disease IX characterized by X-linked inheritance of variable exercise-induced muscle weakness or stiffness that has material basis in mutation in the PHKA1 gene on chromosome Xq13
- glycogenosis type 9D
- glycogen storage disease type 9E
- GSD IXd
- X-linked muscke glycogenosis
- glycogenosis type 9E
- glycogenosis type IXe
- glycogen storage disease type 9D
- GSD type 9E
- GSD type IXd
- glycogenosis type IXd
- glycogen storage disease type IXe
- GSD type IXe
- GSD due to muscle phosphorylase kinase deficiency
- GSD9D
- glycogen storage disease due to muscle phosphorylase kinase deficiency
- muscle phosphorylase kinase deficiency
- glycogenosis due to muscle phosphorylase kinase deficiency
- glycogen storage disease type IXd
- GSD type 9D
- GLYCOGEN STORAGE DISEASE, TYPE IXd
- Muscle Glycogenosis, X-Linked
- Muscular phosphorylase kinase deficiency
- GLYCOGEN STORAGE DISEASE, TYPE IXd; GSD9D
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | glycogen storage disease IXd |
glycogen storage disease IX characterized by X-linked inheritance of variable exercise-induced muscle weakness or stiffness that has material basis in mutation in the PHKA1 gene on chromosome Xq13 |
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