Disease-gene associations mined from literature

Human genes for glycogen storage disease V

Glycogen storage disease V [DOID:2746]

A glycogen storage disease characterized by enlargement of the liver, moderately low blood sugar, elevated levels of acetone and other ketone bodies in the blood and moderate growth retardation.

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

Linkouts:  OMIM