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Disease Ontology Browser
autosomal recessive centronuclear myopathy (DOID:0111216)
Alliance: disease page
Synonyms: AR-CNM
Alt IDs: ORDO:169186
Definition: A centronuclear myopathy that has_material_basis_in autosomal recessive inheritance.


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
11/10/2020
MGI 6.16
The Jackson Laboratory