|Dataset||CTD Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||Oguchi disease is an autosomal recessive retinal disorder characterized by congenital stationary night blindness (see this term) and the Mizuo-Nakamura phenomenon. (Orphanet Rare Disease Ontology, Orphanet_75382)|
|Downloads & Tools|
2 genes/proteins associated with the disease Oguchi disease from the curated CTD Gene-Disease Associations dataset.