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Disease Ontology Browser
myofibrillar myopathy 2 (DOID:0080093)
Alliance: disease page
Synonyms: alpha-b crystallinopathy
Alt IDs: OMIM:608810, ORDO:399058
Definition: A myofibrillar myopathy that has_material_basis_in heterozygous mutation in the alpha-B-crystallin gene on chromosome 11q23.

Disease References using Mouse Models (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
11/12/2024
MGI 6.24 		The Jackson Laboratory