muscular dystrophy-dystroglycanopathy type B2 Disease Ontology Browser

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muscular dystrophy-dystroglycanopathy type B2 (DOID:0112380)
Alliance: disease page
Synonyms: congenital muscular dystrophy POMT2-related; MDDGB2
Alt IDs: OMIM:613156
Definition: A muscular dystrophy-dystroglycanopathy type B that has_material_basis_in homozygous or compound heterozygous mutation in the POMT2 gene on chromosome 14q24.3.

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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