segmental peripheral demyelination Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A loss of myelin from the internode regions along myelinated nerve fibers from segments of the peripheral nervous system. (Human Phenotype Ontology, HP_0007107)
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2 genes associated with the segmental peripheral demyelination phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
DNM2 dynamin 2
SH3TC2 SH3 domain and tetratricopeptide repeats 2