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Disease Ontology Browser
muscular dystrophy-dystroglycanopathy type B15 (DOID:0112376)
Alliance: disease page
Synonyms: congenital muscular dystrophy DPM3-related; MDDGB15
Alt IDs: OMIM:618992
Definition: A muscular dystrophy-dystroglycanopathy type B that has_material_basis_in homozygous or compound heterozygous mutation in the DPM3 gene on chromosome 1q22.

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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 6.22
The Jackson Laboratory