Pure or complex autosomal dominant…

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Pure or complex autosomal dominant spastic paraplegia

ORPHA:320342Clinical group

Also called Pure or complicated autosomal dominant 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

Inheritance
Autosomal dominant
Classified as
Clinical group

Genes reported in subtypes

ALDH18A1ATL1ERLIN2HSPD1KIF1AKIF5ANIPA1REEP1SPASTSPG7WASHC5

Orphanet records these genes on 11 more specific entries under this disorder, not on this entry itself:

Autosomal dominant spastic paraplegia type 10Autosomal dominant spastic paraplegia type 13Autosomal dominant spastic paraplegia type 3Autosomal dominant spastic paraplegia type 31Autosomal dominant spastic paraplegia type 4Autosomal dominant spastic paraplegia type 6Autosomal dominant spastic paraplegia type 8Autosomal dominant spastic paraplegia type 9BAutosomal spastic paraplegia type 18Autosomal spastic paraplegia type 30Spastic paraplegia type 7

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

MONDO 17914UMLS C5679886

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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