Autosomal dominant congenital fibre-type disproportion myopathy due to ACTA1 mutation

Autosomal dominant congenital fiber-type disproportion myopathy due to actin alpha 1, skeletal muscle mutation (disorder)

active

Code	`1208415001`
Semantic tag	disorder
Module	international
Definition	defined
Effective time	20220331

Synonyms

Autosomal dominant congenital fiber-type disproportion myopathy due to actin alpha 1, skeletal muscle mutation
Autosomal dominant congenital fibre-type disproportion myopathy due to actin alpha 1, skeletal muscle mutation

Parents (2)

11164009Autosomal dominant hereditary disorder disorder
1208413008Congenital fibre-type disproportion myopathy due to ACTA1 mutation disorder

Children (0)

None (leaf concept).