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

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

active

Code	`1208414002`
Semantic tag	disorder
Module	international
Definition	defined
Effective time	20220331

Synonyms

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

Parents (2)

85995004Autosomal recessive hereditary disorder disorder
1208413008Congenital fibre-type disproportion myopathy due to ACTA1 mutation disorder

Children (0)

None (leaf concept).