Autosomal dominant spastic paraplegia type 37 (Q100920): 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/1636862745 / rank | |||
Normal rank | |||
Revision as of 17:42, 16 August 2026
A form of hereditary spastic paraplegia characterized by a childhood- to adulthood-onset of slowly progressive spastic gait, extensor plantar responses, brisk tendon reflexes in arms and legs, decreased vibration sense and urinary dysfunction.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1636862745 |
||
| English | Autosomal dominant spastic paraplegia type 37 |
A form of hereditary spastic paraplegia characterized by a childhood- to adulthood-onset of slowly progressive spastic gait, extensor plantar responses, brisk tendon reflexes in arms and legs, decreased vibration sense and urinary dysfunction. |
