hereditary spastic paraplegia 38 (Q32142955)
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hereditary spastic paraplegia that has material basis in variation in the chromosome region 4p16-p15
- autosomal dominant spastic paraplegia 38
- autosomal dominant spastic paraplegia type 38
- SPG38
- hereditary spastic paraplegia type 38
- SPASTIC PARAPLEGIA 38, AUTOSOMAL DOMINANT
- SPASTIC PARAPLEGIA 38, AUTOSOMAL DOMINANT; SPG38
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | hereditary spastic paraplegia 38 |
hereditary spastic paraplegia that has material basis in variation in the chromosome region 4p16-p15 |
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