Rare diseases · Sign or symptom
Impaired proprioception
HP:0010831
What it means
A loss or impairment of the sensation of the relative position of parts of the body and joint position.
Rare diseases that can present with this24
Very common80–99%
3Common30–79%
11- Ataxia with vitamin E deficiency
- Autosomal dominant spastic paraplegia type 12
- Autosomal dominant spastic paraplegia type 19
- Autosomal dominant spastic paraplegia type 31
- Autosomal recessive cerebellar ataxia due to STUB1 deficiency
- Autosomal recessive cerebellar ataxia-movement disorder syndrome
- Autosomal recessive cerebellar ataxia with late-onset spasticity
- Charcot-Marie-Tooth disease type 1F
- Dentatorubral pallidoluysian atrophy
- Maternal uniparental disomy of chromosome 4 syndrome
- Spinocerebellar ataxia type 23
Sometimes5–29%
7The 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: Abnormality of proprioception
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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.