glycogen storage disease vi Gene Set

Dataset DISEASES Text-mining Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
Description A glycogen storage disease characterized by enlargement of the liver, moderately low blood sugar, elevated levels of acetone and other ketone bodies in the blood and moderate growth retardation. (Human Disease Ontology, DOID_2754)
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Genes

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

Symbol Name Standardized Value
PYGL phosphorylase, glycogen, liver 1.7718
PYGM phosphorylase, glycogen, muscle 1.40658
PYGB phosphorylase, glycogen; brain 1.23082
MYH7 myosin, heavy chain 7, cardiac muscle, beta 0.849945
MYH6 myosin, heavy chain 6, cardiac muscle, alpha 0.667947
CHGA chromogranin A 0.366671
FOS FBJ murine osteosarcoma viral oncogene homolog 0.258417