optic nerve hypoplasia and abnormalities of the central nervous system Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
External Link http://www.omim.org/entry/206900
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Genes

1 genes associated with the optic nerve hypoplasia and abnormalities of the central nervous system phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
SOX2 SRY (sex determining region Y)-box 2