|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||A form or retinal dystrophy that is present at birth and does not further progress. (Human Phenotype Ontology, HP_0007910)|
|Downloads & Tools|
1 genes associated with the nonprogressive congenital retinal dystrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
|INPP5E||inositol polyphosphate-5-phosphatase, 72 kDa|