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Disease Ontology Browser
myofibrillar myopathy 1 (DOID:0080092)
Alliance: disease page
Synonyms: autosomal recessive limb-girdle muscular dystrophy type 2R; desminopathy
Alt IDs: OMIM:601419, DOID:0110286, DOID:0110286, DOID:0110286, DOID:0110286, DOID:0110286, DOID:0110286, DOID:0110286, DOID:0110286, DOID:0110286, DOID:0110286, DOID:0110286, DOID:0110286, DOID:0110286, DOID:0110286, DOID:0110286, DOID:0110286, DOID:0110286, DOID:0110286, DOID:0110286, DOID:0110286, DOID:0110286, DOID:0110286, DOID:0110286, DOID:0110286, DOID:0110286, ICD10CM:G71.0, ORDO:363543

Disease References using Mouse Models (5)

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
02/18/2020
MGI 6.14
The Jackson Laboratory