foveal hypoplasia 2, with or without optic nerve misrouting and/or anterior segment dysgenesis Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
External Link http://www.omim.org/entry/609218
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Genes

1 genes associated with the foveal hypoplasia 2, with or without optic nerve misrouting and/or anterior segment dysgenesis phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
SLC38A8 solute carrier family 38, member 8