Congenital myopathy 4A, autosomal dominant

MONDO:0800341

Also known as: CAPM1, CFTD, CFTDM, NEM1, cap myopathy 1, fiber-type disproportion myopathy, congenital, myopathy, congenital, with fiber-type disproportion, nemaline myopathy 1

4 clinical trials for this condition and its sub-types, 0 tagged with Congenital myopathy 4A, autosomal dominant itself.

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Where it sits in the disease tree

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Part of

↑ TPM3-related myopathy (1)

Including sub-types (4) Tagged with Congenital myopathy 4A, autosomal dominant (0)

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