Limb-girdle muscular dystrophy 1F, gene mapped to 7q32.1-32.2 (Q84652): 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/2102590721 / rank | |||
Normal rank | |||
Revision as of 09:59, 15 August 2026
Limb girdle muscular dystrophy, type 1F (LGMD1F) is an autosomal dominant form of LGMD, a group of genetically determined, progressive muscle weakness disorders, in which the pelvic or shoulder girdle musculature is predominantly or primarily involved, and is characterised by weakness of the pelvic and shoulder muscles
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_2102590721 |
||
| English | Limb-girdle muscular dystrophy 1F, gene mapped to 7q32.1-32.2 |
Limb girdle muscular dystrophy, type 1F (LGMD1F) is an autosomal dominant form of LGMD, a group of genetically determined, progressive muscle weakness disorders, in which the pelvic or shoulder girdle musculature is predominantly or primarily involved, and is characterised by weakness of the pelvic and shoulder muscles |
