Rare diseases · Sign or symptom
Sensory axonal neuropathy
HP:0003390
What it means
An axonal neuropathy of peripheral sensory nerves.
Rare diseases that can present with this21
Very common80–99%
4Common30–79%
10- Adult-onset multiple mitochondrial DNA deletion syndrome due to DGUOK deficiency
- Autosomal recessive progressive external ophthalmoplegia
- Autosomal recessive spastic paraplegia type 78
- Friedreich ataxia
- Infantile-onset axonal motor and sensory neuropathy-optic atrophy-neurodegenerative syndrome
- Mutilating hereditary sensory neuropathy with spastic paraplegia
- Recessive mitochondrial ataxia syndrome
- Sandhoff disease, adult form
- Spinocerebellar ataxia type 27A
- Spinocerebellar ataxia with epilepsy
Sometimes5–29%
6The range is how often this sign appears among people diagnosed with each disease — it is not a probability of having any of them. Many of these signs also occur in common, non-rare conditions. A sign on this page is a conversation to have with a clinician, not a conclusion.
Part of the broader category
Also called: Axonal sensory neuropathy · Peripheral sensory axonal neuropathy
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Start free with EleplanThis page uses the Human Phenotype Ontology (2026-06-23) — Human Phenotype Ontology Consortium, hpo.jax.org. Disease associations from Orphanet (INSERM), CC BY 4.0. Content is educational and is not medical advice.