Autosomal dominant congenital fibre-type disproportion myopathy due to TPM3 mutation

Autosomal dominant congenital fiber-type disproportion myopathy due to tropomyosin 3 mutation (disorder)

active

Code	`1208418004`
Semantic tag	disorder
Module	international
Definition	defined
Effective time	20220331

Synonyms

Autosomal dominant congenital fiber-type disproportion myopathy due to tropomyosin 3 mutation
Autosomal dominant congenital fibre-type disproportion myopathy due to tropomyosin 3 mutation

Parents (2)

11164009Autosomal dominant hereditary disorder disorder
1208416000Congenital fibre-type disproportion myopathy due to TPM3 mutation disorder

Children (0)

None (leaf concept).