retinal dystrophy, early-onset, and pituitary dysfunction Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
External Link http://www.omim.org/entry/610125
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Genes

1 genes associated with the retinal dystrophy, early-onset, and pituitary dysfunction phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
OTX2 orthodenticle homeobox 2