WormBase Tree Display for DO_term: DOID:0111220

DOID:0111220 Name: centronuclear myopathy 2
  Status: Valid
  Definition: An autosomal recessive centronuclear myopathy that has_material_basis_in homozygous or compound heterozygous mutation in BIN1 on 2q14.3.
  Synonym: Exact: CNM2
  Parent: Is_a: DOID:0111216
  DB_info: Database: OMIM disease 255200
  Attribute_of: Gene_by_orthology: WBGene00010272