Autosomal recessive spastic paraplegia type 11 (Q99420): Difference between revisions
From determinar.ia.br - Determine suas informações
Changed label, description and/or aliases in pt-br, en |
Changed an Item |
||
| Property / Canonical URI | |||
| Property / Canonical URI: https://id.who.int/icd/entity/2049927049 / rank | |||
Normal rank | |||
Revision as of 16:05, 16 August 2026
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. |
