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Disease Ontology Browser
centronuclear myopathy 4 (DOID:0111224)
Alliance: disease page
Synonyms: CNM4
Alt IDs: OMIM:614807
Definition: An autosomal dominant centronuclear myopathy that has_material_basis_in heterozygous mutation in CCDC78 on 16p13.3.

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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last database update
MGI 6.17
The Jackson Laboratory