optic nerve hypoplasia Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Underdevelopment of the optic nerve. (Human Phenotype Ontology, HP_0000609)
External Link http://www.omim.org/entry/165550
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1 genes associated with the optic nerve hypoplasia phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
PAX6 paired box 6