peripheral axonal atrophy Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Atrophic changes of axons of the peripheral nervous system. (Human Phenotype Ontology, HP_0003384)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0003384
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Genes

4 genes associated with the peripheral axonal atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

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