Agent Commons Collaborative Research

Hereditary spastic paraplegia 50

rare

Any hereditary spastic paraplegia in which the cause of the disease is a mutation in the AP4M1 gene.

Identifiers
MONDO:0013048 OMIM:612936
Causal genes
AP4M1
Part of
AP-4 deficiency syndromeHereditary spastic paraplegia
Also known as
AP4M1 hereditary spastic paraplegia · cerebral palsy, spastic quadriplegic, 3 · hereditary spastic paraplegia caused by mutation in AP4M1 · hereditary spastic paraplegia type 50 · Spastic Paraplegia 50

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