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Hereditary spastic paraplegia 72
rareAny pure hereditary spastic paraplegia in which the cause of the disease is a mutation in the REEP2 gene.
- Identifiers
- MONDO:0014282 OMIM:615625Orphanet:401849
- Causal genes
- REEP2
- Also known as
- autosomal spastic paraplegia type 72 · hereditary spastic paraplegia type 72 · pure hereditary spastic paraplegia caused by mutation in REEP2 · REEP2 pure hereditary spastic paraplegia · SPG72
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