Peripheral Axonal Atrophy Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description Atrophic changes of axons of the peripheral nervous system. (Human Phenotype Ontology, HP_0003384)
External Link https://www.disgenet.org/browser/0/1/0/C4025619
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Genes

4 genes associated with the disease Peripheral Axonal Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
KIF1B kinesin family member 1B
LMNA lamin A/C
MFN2 mitofusin 2
RAB7A RAB7A, member RAS oncogene family