Human genes for glycogen storage disease XV
Glycogen storage disease XV [DOID:0050579]
A glycogen storage disease characterized by muscle weakness and cardiac abnormalities caused and has_material_basis_in mutation in the GYG1 gene that encodes glycogenin-1.
Synonyms: glycogen storage disease XV, DOID:0050579, glycogen storage disease XVs, Glycogen storage disease 15, Glycogen storage disease with severe cardiomyopathy due to glycogenin deficiency ...
Linkouts: OMIM