Preferred Label : Limb-girdle muscular dystrophy 1A, myotilin myopathy;
ICD-11 definition : Autosomal dominant limb-girdle muscular dystrophy type 1A 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 1A is characterized
by dysarthria and has not been associated with cardiac problems, with onset in young
adulthood.;
ICD-11 synonym : LGMD 1A - [Limb-girdle muscular dystrophy 1A, myotilin myopathy];
ICD-11 acronym : LGMD 1A;
Origin ID : 172327936;
Currated CISMeF NLP mapping
Autosomal dominant limb-girdle muscular dystrophy type 1A 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 1A is characterized
by dysarthria and has not been associated with cardiac problems, with onset in young
adulthood.
