Disease-gene associations mined from literature

Human genes for glycogen storage disease V

Glycogen storage disease V [DOID:2746]

Glycogen storage disease type V (GSD-V) is a metabolic disorder, more specifically a glycogen storage disease, caused by a deficiency of myophosphorylase. Its incidence is reported as 1 in 100,000, approximately the same as glycogen storage disease type I.

Synonyms:  glycogen storage disease V,  DOID:2746,  Glycogen storage disease, type V (disorder),  McArdle's disease,  glycogen storage disease type V ...

Linkouts:  OMIM