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 )

Relationships
is a type of: autosomal recessive centronuclear myopathy