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Download Data for glycogen storage disease due to hepatic glycogen synthase deficiency
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Counts of Target Development Levels for diseases known to be associated with this disease. If the disease has a valid DOID, targets known to be associated with all child diseases are aggregated. Click "Explore Associated Targets" to view more facets and details for the target list.
This disease has been annotated by GARD as a rare disease.
Description from Mondo Disease Ontology.
Description from UniProt.
DataSources which have contributed target associations to this disease, and the identifiers by which the disease is referenced.
GARD:0002513
GARD:0002889
MESH:C565485
OMIM:240600
Orphanet:2089
SCTID:237964009
UMLS:C0342748
UMLS:C1855861
MONDO:0009414
High level summary of knowledge for a disease, including descriptions and datasource references.
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Opens the Target List with this set of targets