Skip to content
Use your HSA or FSA funds

Trait

Chronic axonal neuropathy

An abnormality characterized by chronic impairment of the normal functioning of the axons.

HPO HP:0007267

Summary

Also called
Chronic sural axonal neuropathy
Body system
Abnormality of the nervous system

7 genes linked to Chronic axonal neuropathy

Changes in these genes cause rare conditions in which Chronic axonal neuropathy is seen. Most people with this trait have none of those conditions, and a gene on this list says nothing about anyone's own genome.

GeneHow often it is seenConditions
COG8component of oligomeric golgi complex 8AlwaysIn 2 conditions
GDAP1ganglioside induced differentiation associated protein 1Very often (80–99%)In 2 conditions
SYNE1spectrin repeat containing nuclear envelope protein 1Sometimes (5–29%)In 1 condition
HSPB1heat shock protein family B (small) member 1Not recordedIn 1 condition
KCNJ10potassium inwardly rectifying channel subfamily J member 10Not recordedIn 1 condition
SETXsenataxinNot recordedIn 1 condition
SPTLC1serine palmitoyltransferase long chain base subunit 1Not recordedIn 1 condition

How often is among people with one of the gene's conditions, the most often across them, as the Human Phenotype Ontology records it. These pages describe traits and the research behind them; they are not a diagnosis, and a doctor or genetic counsellor is the person to ask about symptoms.

Broader traits

Peripheral axonal neuropathy

Where this comes from

  • The Human Phenotype Ontology, release 2026-09-01: the trait, its names, its definition and the genes linked to it. Find out more at hpo.jax.org.
  • Data release 2026.10.16-c6eea6bf.

One test. A lifetime of answers.

From $449Free shipping · Results in 6–8 weeks

Get my Genome Test