(Q32142692)
English
hereditary spastic paraplegia 19
hereditary spastic paraplegia that has material basis in variation in the chromosome region 9q
- autosomal dominant spastic paraplegia 19
- SPG19
- autosomal dominant spastic paraplegia type 19
- hereditary spastic paraplegia type 19
- SPASTIC PARAPLEGIA 19, AUTOSOMAL DOMINANT; SPG19
- SPASTIC PARAPLEGIA 19, AUTOSOMAL DOMINANT
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