hereditary spastic paraplegia 24
MONDO:0011862Mondo
Findings
No curated finding names hereditary spastic paraplegia 24 yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
A hereditary spastic paraplegia that has material basis in variation in the chromosome region 13q14.
Definition from the Mondo Disease Ontology (MONDO:0011862), read 2026-09-29. CC BY 4.0.
Features
7 features
What the disease is reported to present with, and how often among people who have it — never how often a feature means the disease. HPO, annotations 2026-09-02.
- ClonusHPOHP:0002169
- Very frequent (80% to 99% of cases)
- HyperreflexiaHPOHP:0001347
- Very frequent (80% to 99% of cases)
- Scissor gaitHPOHP:0012407
- Very frequent (80% to 99% of cases)
- Spastic paraplegiaHPOHP:0001258
- Very frequent (80% to 99% of cases)
- SpasticityHPOHP:0001257
- Very frequent (80% to 99% of cases)
- Tip-toe gaitHPOHP:0030051
- Very frequent (80% to 99% of cases)
- Sensorineural hearing impairmentHPOHP:0000407
- Frequent (30% to 79% of cases)
Where it sits
Other names
3 names
Resolves to: hereditary spastic paraplegia 24
- Also called
- autosomal recessive spastic paraplegia type 24hereditary spastic paraplegia type 24SPG24