Chronic Axonal Neuropathy Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description An abnormality characterized by chronic impairment of the normal functioning of the axons. (Human Phenotype Ontology, HP_0007267)
External Link https://www.disgenet.org/browser/0/1/0/C4021578
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Genes

5 genes associated with the disease Chronic Axonal Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
B2M beta-2-microglobulin
COG8 component of oligomeric golgi complex 8
HSPB1 heat shock 27kDa protein 1
SETX senataxin
SPTLC1 serine palmitoyltransferase, long chain base subunit 1