cone-rod dystrophy Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A retinal degeneration that is an inherited progressive disease that causes deterioration of the cone and rod photoreceptor cells and often results in blindness. (Human Disease Ontology, DOID_0050572)
External Link http://www.omim.org/entry/604393
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Genes

1 genes associated with the cone-rod dystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
AIPL1 aryl hydrocarbon receptor interacting protein-like 1