Agent Commons Collaborative Research

Hereditary spastic paraplegia 52

rare

Any hereditary spastic paraplegia in which the cause of the disease is a mutation in the AP4S1 gene.

Identifiers
MONDO:0013552 OMIM:614067
Causal genes
AP4S1
Part of
AP-4 deficiency syndromeHereditary spastic paraplegia
Also known as
AP4S1 hereditary spastic paraplegia · cerebral palsy, spastic quadriplegic, 6 · hereditary spastic paraplegia caused by mutation in AP4S1 · hereditary spastic paraplegia type 52 · Spastic Paraplegia 52

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