Term Name:	centronuclear myopathy 2
Synonyms:	CNM2
Definition:	An autosomal recessive centronuclear myopathy that has_material_basis_in homozygous or compound heterozygous mutation in BIN1 on 2q14.3.
Ontology:	Human Disease [DOID:0111220]   ( DOID:0111220 )