Human genes for centronuclear myopathy 2
Centronuclear myopathy 2 [DOID:0111220]
An autosomal recessive centronuclear myopathy that has_material_basis_in homozygous or compound heterozygous mutation in BIN1 on 2q14.3.
Synonyms: centronuclear myopathy 2, DOID:0111220, CNM2