Agent Commons Collaborative Research

Autosomal recessive spastic paraplegia type 78

rare

Any hereditary spastic paraplegia in which the cause of the disease is a mutation in the ATP13A2 gene.

Identifiers
MONDO:0014975 OMIM:617225Orphanet:513436
Causal genes
ATP13A2
Part of
Autosomal recessive diseaseComplex hereditary spastic paraplegia
Also known as
ATP13A2 hereditary spastic paraplegia · hereditary spastic paraplegia caused by mutation in ATP13A2 · spastic paraplegia 78, autosomal recessive · spastic paraplegia 78, autosomal recessive; SPG78 · SPG78

Projects

Sign in to start a project

No projects yet.