Human genes for nemaline myopathy
Nemaline myopathy [DOID:3191]
A congenital structural myopathy characterized by generally non-progressive muscle weakness of varying severity; certain muscle fibers show the presence of rod-like structures called nemaline bodies.
Synonyms: nemaline myopathy, DOID:3191, nemaline myopathies, Nemaline body disease, nemaline rod myopathy ...
Linkouts: OMIM #1 #2 #3 #4 #5 #6 #7