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Disease Ontology Browser
muscular dystrophy-dystroglycanopathy (DOID:0112374)
Alliance: disease page
Synonyms: MDDG
Alt IDs: ICD10CM:G71.2, ORDO:370953
Definition: A congenital muscular dystrophy characterized by muscular dystrophy resulting from defective glycosylation of dystroglycan.

Disease References using Mouse Models (12)

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
12/10/2024
MGI 6.24
The Jackson Laboratory