hereditary spastic paraplegia 41 (Q32143002)
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A hereditary spastic paraplegia that has material basis in variation in the chromosome region 11p14.1-p11.2.
- autosomal dominant spastic paraplegia 41
- autosomal dominant spastic paraplegia type 41
- SPG41
- SPASTIC PARAPLEGIA 41, AUTOSOMAL DOMINANT; SPG41
- SPASTIC PARAPLEGIA 41, AUTOSOMAL DOMINANT
- hereditary spastic paraplegia type 41
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | hereditary spastic paraplegia 41 |
A hereditary spastic paraplegia that has material basis in variation in the chromosome region 11p14.1-p11.2. |
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Statements
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Identifiers
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