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Summary Literature (0)
MIM:255995 - CONGENITAL MYOPATHY 13; CMYO13

Xenbase Genes: stac3

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0009722 - entire pharyngeal arch endoderm

Disease Ontology (DO):
DOID:0060346 - congenital myopathy 13