Dataset | OMIM Gene-Disease Associations |
Category | disease or phenotype associations |
Type | phenotype |
External Link | http://www.omim.org/entry/615287 |
Similar Terms | |
Downloads & Tools |
1 genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 13 phenotype from the curated OMIM Gene-Disease Associations dataset.
Symbol | Name |
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B3GNT1 |