Hepatorenal form of glycogen storage disease [Supplementary Concept]
Type I glycogen storage disease (OMIM: 232200) that is associated with mutations in the G6PC gene (OMIM: 613742.0001-OMIM: 613742.0014).
Date introduced: August 25, 2010
MeSH Unique ID: C538655
Heading Mapped to:
Entry Terms:
- Glycogen storage disease type IA
- Hepatorenal glycogenosis