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

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

active

Code	`1202025005`
Semantic tag	disorder
Module	international
Definition	defined
Effective time	20220228

Synonyms

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

Parents (4)

85995004Autosomal recessive 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).