demyelinating peripheral neuropathy Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Demyelinating neuropathy is characterized by slow nerve conduction velocities with reduced amplitudes of sensory/motor nerve conduction and prolonged distal latencies. (Human Phenotype Ontology, HP_0007108)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0007108
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Genes

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

Symbol Name
ACO2 aconitase 2, mitochondrial
BAG3 BCL2-associated athanogene 3
GJC2 gap junction protein, gamma 2, 47kDa
MANBA mannosidase, beta A, lysosomal
PMP22 peripheral myelin protein 22
SOX10 SRY (sex determining region Y)-box 10