Rare diseases · Sign or symptom
Spinal cord lesion
HP:0100561
Rare diseases that can present with this14
Common30–79%
9- Autosomal dominant spastic paraplegia type 12
- Autosomal dominant spastic paraplegia type 19
- Autosomal dominant spastic paraplegia type 37
- Autosomal dominant spastic paraplegia type 38
- Autosomal dominant spastic paraplegia type 41
- Autosomal dominant spastic paraplegia type 42
- Autosomal dominant spastic paraplegia type 8
- Caudal duplication
- Childhood-onset spasticity with hyperglycinemia
The 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
Spinal cord lesion
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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.