demyelinating motor neuropathy Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Demyelination of peripheral motor nerves. (Human Phenotype Ontology, HP_0007220)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0007220
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Genes

1 genes associated with the demyelinating motor neuropathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
GJC2 gap junction protein, gamma 2, 47kDa