glycogen storage disease iii Gene Set

Dataset DISEASES Text-mining Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
Description OMIM mapping confirmed by DO. [SN]. (Human Disease Ontology, DOID_2748)
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Genes

10 genes co-occuring with the disease glycogen storage disease iii in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
AGL amylo-alpha-1, 6-glucosidase, 4-alpha-glucanotransferase 2.20363
PYGB phosphorylase, glycogen; brain 1.41183
PYGL phosphorylase, glycogen, liver 1.40789
PYGM phosphorylase, glycogen, muscle 1.37774
GAA glucosidase, alpha; acid 0.8741
GBE1 glucan (1,4-alpha-), branching enzyme 1 0.839705
SLC37A4 solute carrier family 37 (glucose-6-phosphate transporter), member 4 0.791311
G6PC glucose-6-phosphatase, catalytic subunit 0.57305
PFKM phosphofructokinase, muscle 0.518034
GCG glucagon 0.316456