Autosomal recessive spastic paraplegia type 11 (Q99420)
From determinar.ia.br - Determine suas informações
A recessive genetic disorder secondary to mutation of the SPG11 gene, which manifests as progressive lower extremity spasticity and paralysis of the lower limb.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_2049927049 |
||
| English | Autosomal recessive spastic paraplegia type 11 |
A recessive genetic disorder secondary to mutation of the SPG11 gene, which manifests as progressive lower extremity spasticity and paralysis of the lower limb. |
Statements
CID11:ID_2049927049
0 references
