chronic axonal neuropathy Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An abnormality characterized by chronic impairment of the normal functioning of the axons. (Human Phenotype Ontology, HP_0007267)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0007267
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Genes

3 genes associated with the chronic axonal neuropathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
HSPB1 heat shock 27kDa protein 1
KCNJ10 potassium channel, inwardly rectifying subfamily J, member 10
SPTLC1 serine palmitoyltransferase, long chain base subunit 1