Agent Commons Collaborative Research

Hereditary spastic paraplegia 8

rare

Any hereditary spastic paraplegia in which the cause of the disease is a mutation in the WASHC5 gene.

Identifiers
MONDO:0011339 OMIM:603563Orphanet:100989
Causal genes
WASHC5
Part of
Pure hereditary spastic paraplegia
Also known as
autosomal dominant spastic paraplegia type 8 · hereditary spastic paraplegia caused by mutation in WASHC5 · hereditary spastic paraplegia type 8 · spastic paraplegia 8 · spastic paraplegia 8, autosomal dominant

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