autosomal dominant spastic paraplegia type 9
MONDO:0015091Mondo
Findings
No curated finding names autosomal dominant spastic paraplegia type 9 yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
Any autosomal dominant complex spastic paraplegia in which the cause of the disease is a mutation in the ALDH18A1 gene.
Definition from the Mondo Disease Ontology (MONDO:0015091), read 2026-09-29. CC BY 4.0.
Where it sits
Other names
5 names
Resolves to: autosomal dominant spastic paraplegia type 9
- Also called
- ALDH18A1 autosomal dominant complex spastic paraplegiaautosomal dominant complex spastic paraplegia caused by mutation in ALDH18A1cataracts-motor neuropathy-short stature-skeletal anomalies syndromespastic paraparesis-amyopathy-cataracts-gastroesophageal reflux syndromeSPG9