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Spastic paraplegia 82, autosomal recessive
rareAny hereditary spastic paraplegia in which the cause of the disease is an autosomal recessive mutation in the PCYT2 gene.
- Identifiers
- MONDO:0032906 OMIM:618770Orphanet:631073
- Causal genes
- PCYT2
- Part of
- Hereditary spastic paraplegia
- Also known as
- autosomal recessive spastic paraplegia type 82 · SPG82
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