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MIM:255310 - CONGENITAL MYOPATHY 4A, AUTOSOMAL DOMINANT; CMYP4A
Xenbase Genes: acta1, myh7, selenon, ryr1, tpm2, tpm3
Human Disease Resource: OMIM
MONDO:0009711 - congenital fiber-type disproportion myopathy |
DOID:0080102 - congenital myopathy 4A |
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MONDO:0009711 - congenital fiber-type disproportion myopathy |
DOID:0080102 - congenital myopathy 4A |