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Hereditary spastic paraplegia 51

rare

Any hereditary spastic paraplegia in which the cause of the disease is a mutation in the AP4E1 gene.

Identifiers
MONDO:0013401 OMIM:613744
Causal genes
AP4E1
Part of
AP-4 deficiency syndromeHereditary spastic paraplegia
Also known as
AP4E1 hereditary spastic paraplegia · cerebral palsy, spastic quadriplegic, 4 · hereditary spastic paraplegia caused by mutation in AP4E1 · hereditary spastic paraplegia type 51 · Spastic Paraplegia 51

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