Facioscapulohumeral muscular dystrophy 2

Any facioscapulohumeral muscular dystrophy in which the cause of the disease is a mutation in the SMCHD1 gene.

Also known as: SMCHD1 facioscapulohumeral muscular dystrophy, facioscapulohumeral muscular dystrophy 2, facioscapulohumeral muscular dystrophy caused by mutation in SMCHD1, facioscapulohumeral muscular dystrophy type 2, fascioscapulohumeral muscular dystrophy 2, digenic, digenic dominant, FSHD2, Fshd2, digenic, facioscapulohumeral muscular dystrophy 2, digenic

12 clinical trials for this condition and its sub-types.