glycogen storage disease IX
MONDO:0700291Mondo
Findings
No curated finding names glycogen storage disease IX yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
A group of inborn errors of glycogen metabolism that is clinically and genetically heterogeneous. This group comprises GSD due to liver phosphorylase kinase (PhK) deficiency, GSD due to muscle PhK deficiency and GSD due to liver and muscle PhK deficiency.
Definition from the Mondo Disease Ontology (MONDO:0700291), read 2026-09-29. CC BY 4.0.
Where it sits
- A kind of
Other names
12 names
Resolves to: glycogen storage disease IX
- Also called
- glycogen storage disease 9glycogen storage disease type 9glycogen storage disease type IXglycogenosis due to phosphorylase kinase deficiencyglycogenosis type 9glycogenosis type IXGSD IXGSD type 9GSD type IXGSD9GSDIXphosphorylase kinase deficiency