nonprogressive congenital retinal dystrophy Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A form or retinal dystrophy that is present at birth and does not further progress. (Human Phenotype Ontology, HP_0007910)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0007910
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Genes

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.

Symbol Name
INPP5E inositol polyphosphate-5-phosphatase, 72 kDa