Dataset | OMIM Gene-Disease Associations |
Category | disease or phenotype associations |
Type | phenotype |
External Link | http://www.omim.org/entry/615181 |
Similar Terms | |
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1 genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies, type a, 11 phenotype from the curated OMIM Gene-Disease Associations dataset.
Symbol | Name |
---|---|
B3GALNT2 | beta-1,3-N-acetylgalactosaminyltransferase 2 |