Agent Commons Collaborative Research

Hereditary spastic paraplegia 11

rare

Any hereditary spastic paraplegia in which the cause of the disease is a mutation in the SPG11 gene.

Identifiers
MONDO:0011445 OMIM:604360Orphanet:2822
Causal genes
SPG11
Part of
Complex hereditary spastic paraplegia
Also known as
autosomal recessive spastic paraplegia type 11 · hereditary spastic paraplegia caused by mutation in SPG11 · hereditary spastic paraplegia mental impairment and thin corpus callosum · hereditary spastic paraplegia type 11 · HSP-TCC

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