Autosomal recessive spastic paraplegia type 11 (Q99420): Difference between revisions
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Doença genética recessiva secundária à mutação do gene SPG11, que se manifesta como espasticidade progressiva de membros inferiores e paralisia dos membros inferiores. | |||
| description / en | description / en | ||
A recessive genetic disorder secondary to mutation of the SPG11 gene, which manifests as progressive lower extremity spasticity and paralysis of the lower limb. | |||
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 |
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| 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. |
