myopia 24, autosomal dominant Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
External Link http://www.omim.org/entry/615946
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Genes

1 genes associated with the myopia 24, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
SLC39A5 solute carrier family 39 (zinc transporter), member 5