demyelination Gene Set

Dataset GAD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A loss of myelin from the internode regions along myelinated nerve fibers of the peripheral nervous system. (Human Phenotype Ontology, HP_0011096)
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Genes

1 genes associated with the disease demyelination in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Symbol Name
MPZ myelin protein zero