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Summary Literature (0)
MIM:181430 - MOVED TO 608358

Xenbase Genes: myh7l

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0008409 - congenital myopathy 7A, myosin storage, autosomal dominant

Disease Ontology (DO):
DOID:0060253 - scapuloperoneal myopathy