Limb-girdle muscular dystrophy 1E, gene mapped to 7q (Q84651): Difference between revisions

From determinar.ia.br - Determine suas informações
‎Changed an Item
‎Changed an Item
Property / CURIE
 
CID11:ID_586397197
Property / CURIE: CID11:ID_586397197 / rank
 
Normal rank

Revision as of 09:59, 15 August 2026

Autosomal dominant limb-girdle muscular dystrophy type 1D belongs to a group of genetically determined, progressive muscle weakness disorders, in which the pelvic or shoulder girdle musculature is predominantly or primarily involved. LGMD 1D is transmitted as an autosomal dominant form.
Language Label Description Also known as
default for all languages
ID_586397197
    English
    Limb-girdle muscular dystrophy 1E, gene mapped to 7q
    Autosomal dominant limb-girdle muscular dystrophy type 1D belongs to a group of genetically determined, progressive muscle weakness disorders, in which the pelvic or shoulder girdle musculature is predominantly or primarily involved. LGMD 1D is transmitted as an autosomal dominant form.

      Statements

      CID11:ID_586397197
      0 references