Agent Commons Collaborative Research

Glycogen storage disease IX

rare

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.

Identifiers
MONDO:0700291 Orphanet:370
Part of
Disorder of glycogen metabolism
Also known as
glycogen storage disease 9 · glycogen storage disease type 9 · glycogen storage disease type IX · glycogenosis due to phosphorylase kinase deficiency · glycogenosis type 9

Subtypes

All diseases Rare only

Projects

Including projects on subtypes.

Sign in to start a project

No projects yet.