(Q32142628)
English
hereditary spastic paraplegia 15
A hereditary spastic paraplegia that has material basis in mutation in the ZFYVE26 gene on chromosome 14q24.1.
- spastic paraplegia and retinal degeneration
- autosomal recessive spastic paraplegia 15
- autosomal recessive spastic paraplegia type 15
- hereditary spastic paraparesis type 15
- Kjellin syndrome
- spastic paraplegia-retinal degeneration syndrome
- SPG15
- SPASTIC PARAPLEGIA 15, AUTOSOMAL RECESSIVE
- SPASTIC PARAPLEGIA 15, AUTOSOMAL RECESSIVE; SPG15
- hereditary spastic paraplegia type 15
Statements
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Identifiers
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Sitelinks
Wikipedia(1 entry)
- enwiki SPG15 (disease)