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Summary Literature (0)
MIM:255310 - CONGENITAL MYOPATHY 4A, AUTOSOMAL DOMINANT; CMYP4A

Xenbase Genes: acta1, myh7l, selenon, ryr1, tpm2, tpm3

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0009711 - congenital fiber-type disproportion myopathy

Disease Ontology (DO):
DOID:0080102 - congenital myopathy 4A