(Q32146382)
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
- 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
Statements
1 reference
1 reference
1 reference
3 references
1 reference
Identifiers
1 reference
1 reference
1 reference
2 references
1 reference
1 reference
1 reference