muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type b, 2 Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
External Link http://www.omim.org/entry/613156
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Genes

1 genes associated with the muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type b, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
POMT2 protein-O-mannosyltransferase 2