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Summary Literature (1)
MIM:158901 - FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY 2, DIGENIC; FSHD2

Xenbase Genes: smchd1

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0001347 - facioscapulohumeral muscular dystrophy
MONDO:0008031 - facioscapulohumeral muscular dystrophy 2

Disease Ontology (DO):
DOID:0111193 - facioscapulohumeral muscular dystrophy 2
DOID:11727 - facioscapulohumeral muscular dystrophy