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Start free with EleplanAutosomal dominant pure spastic paraplegia
ORPHA:100980Clinical group
Also called Autosomal dominant pure HSP · Autosomal dominant pure SPG · Autosomal dominant uncomplicated HSP · Autosomal dominant uncomplicated SPG · Autosomal dominant uncomplicated spastic paraplegia
What it is
Orphanet has not published a description for this disease yet. The identifiers, classification and cross-references below are still current.
Key facts
- Prevalence
- 1-9 / 1 000 000 (Ireland)
- Inheritance
- Autosomal dominant
- Classified as
- Clinical group
Prevalence figures describe populations, not individuals, and are often estimates from a single study. Where the figure is an incidence or a birth prevalence, it says so.
Genes reported in subtypes
Orphanet records these genes on 10 more specific entries under this disorder, not on this entry itself:
A well-studied disease is usually split into subtypes, and the gene is curated on whichever one the evidence belongs to. Open a subtype to see which gene goes with it.
Cross-references
Orphadata Science: Free access data from Orphanet. © INSERM 1999. Data version 2026-06-23. Available under CC BY 4.0. This is a reference, not medical advice.
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