Septo-Optic Dysplasia Gene Set

Dataset HuGE Navigator Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description Underdevelopment of the optic nerve and absence of the septum pellucidum. (Human Phenotype Ontology, HP_0100842)
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6 genes associated with the Septo-Optic Dysplasia phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Symbol Name
ANOS1 anosmin 1
FGF8 fibroblast growth factor 8 (androgen-induced)
FGFR1 fibroblast growth factor receptor 1
HESX1 HESX homeobox 1
PROK2 prokineticin 2
PROKR2 prokineticin receptor 2