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Disease Ontology Browser
centronuclear myopathy 2 (DOID:0111220)
Alliance: disease page
Synonyms: CNM2
Alt IDs: OMIM:255200, MESH:C562934, UMLS_CUI:C0410204
Definition: An autosomal recessive centronuclear myopathy that has_material_basis_in homozygous or compound heterozygous mutation in BIN1 on 2q14.3.

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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Send questions and comments to User Support. 		last database update
10/22/2024
MGI 6.24 		The Jackson Laboratory