Facioscapulohumeral muscular dystrophy 2

MONDO:0008031

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

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