MeSH Browser

MeSH Supplementary: Hepatorenal form of glycogen storage disease
Unique ID: C538655
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C538655
Entry Term(s): Glycogen storage disease type IA; Hepatorenal glycogenosis
Registry Numbers: 0
Heading Mapped to: *Glycogen Storage Disease Type I
Frequency: 91
Note: Type I glycogen storage disease (OMIM: 232200) that is associated with mutations in the G6PC gene (OMIM: 613742.0001-OMIM: 613742.0014).
Date of Entry: 2010/08/25
Revision Date: 2016/08/01

Hepatorenal form of glycogen storage disease MeSH Supplementary Concept Data 2025