/congenital myopathy 4A, autosomal dominant

congenital myopathy 4A, autosomal dominant

Rare Disease

MONDO:0800341

Also Known As

CAPM1CFTDCFTDMNEM1cap myopathy 1fiber-type disproportion myopathy, congenitalmyopathy, congenital, with fiber-type disproportionnemaline myopathy 1

Comprehensive, easy-to-understand information about this condition

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Gene data from MyGene.info • Click to view on NCBI Gene

congenital myopathy 4B, autosomal recessive

MONDO:0012239

cap myopathy

MONDO:0015753