autosomal dominant complex spastic paraplegia
MONDO:0015087Mondo
Findings
No curated finding names autosomal dominant complex spastic paraplegia yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
Autosomal dominant form of complex hereditary spastic paraplegia.
Definition from the Mondo Disease Ontology (MONDO:0015087), read 2026-09-29. CC BY 4.0.
Where it sits
- Narrower terms (13)
- autosomal dominant spastic paraplegia type 9
- hereditary spastic paraplegia 17
- hereditary spastic paraplegia 29
- hereditary spastic paraplegia 36
- hereditary spastic paraplegia 38
- spastic paraplegia 18a, autosomal dominant
- spastic paraplegia-epilepsy-intellectual disability syndrome
- spastic paraplegia-facial-cutaneous lesions syndrome
- spastic paraplegia-nephritis-deafness syndrome
- spastic paraplegia-neuropathy-poikiloderma syndrome
- spastic paraplegia-Paget disease of bone syndrome
- spastic paraplegia-precocious puberty syndrome
- spastic paraplegia, intellectual disability, nystagmus, and obesity
Other names
7 names
Resolves to: autosomal dominant complex spastic paraplegia
- Also called
- autosomal dominant complex hereditary spastic paraplegiaautosomal dominant complex HSPautosomal dominant complex SPGautosomal dominant complicated HSPautosomal dominant complicated spastic paraplegiaautosomal dominant complicated SPGcomplex hereditary spastic paraplegia, autosomal dominant