Human genes for centronuclear myopathy 1
Centronuclear myopathy 1 [DOID:0111223]
An autosomal dominant centronuclear myopathy characterized by slowly progressive muscle wasting and weakness involving mainly the limb girdle, trunk, and neck muscles that has_material_basis_in heterozygous mutation in DNM2 on 19p13.2.
Synonyms: centronuclear myopathy 1, DOID:0111223, CNM1