Congenital myopathy 4A, autosomal dominant
MONDO:0800341Also known as: CAPM1, CFTD, CFTDM, NEM1, cap myopathy 1, fiber-type disproportion myopathy, congenital, myopathy, congenital, with fiber-type disproportion, nemaline myopathy 1
37 clinical trials for this condition and its sub-types.
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