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

Autosomal dominant congenital fiber-type disproportion myopathy due to selenoprotein N mutation (disorder)

active

Code	`1202024009`
Semantic tag	disorder
Module	international
Definition	defined
Effective time	20220228

Synonyms

Autosomal dominant congenital fiber-type disproportion myopathy due to selenoprotein N mutation
Autosomal dominant congenital fibre-type disproportion myopathy due to selenoprotein N mutation

Parents (4)

11164009Autosomal dominant hereditary disorder disorder
1202023003Congenital fibre-type disproportion myopathy due to SELENON mutation disorder
363070008Developmental hereditary disorder disorder
363212003Hereditary disorder of musculoskeletal system disorder

Children (0)

None (leaf concept).