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Facioscapulohumeral muscular dystrophy 2
rareAny facioscapulohumeral muscular dystrophy in which the cause of the disease is a mutation in the SMCHD1 gene.
- Identifiers
- MONDO:0008031 OMIM:158901
- Causal genes
- SMCHD1DUX4
- Also known as
- facioscapulohumeral muscular dystrophy caused by mutation in SMCHD1 · facioscapulohumeral muscular dystrophy type 2 · fascioscapulohumeral muscular dystrophy 2, digenic, digenic dominant · FSHD2 · SMCHD1 facioscapulohumeral muscular dystrophy
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