hereditary spastic paraplegia 29 (Q32142811)
Jump to navigation
Jump to search
A hereditary spastic paraplegia that has material basis in variation in the chromosome region 1p31.1-p21.1.
- SPG29
- autosomal dominant spastic paraplegia 29
- Autosomal dominant spastic paraplegia type 29
- SPASTIC PARAPLEGIA 29, AUTOSOMAL DOMINANT
- SPASTIC PARAPLEGIA 29, AUTOSOMAL DOMINANT; SPG29
- hereditary spastic paraplegia type 29
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | hereditary spastic paraplegia 29 |
A hereditary spastic paraplegia that has material basis in variation in the chromosome region 1p31.1-p21.1. |
|
Statements
1 reference
1 reference
1 reference
1 reference
Identifiers
1 reference
1 reference
1 reference
2 references
1 reference
1 reference