peripapillary chorioretinal atrophy Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Chorioretinal atrophy concentrated around the optic papilla (i.e., the optic nerve head). (Human Phenotype Ontology, HP_0007950)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0007950
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Genes

2 genes associated with the peripapillary chorioretinal atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
NRL neural retina leucine zipper
TEAD1 TEA domain family member 1 (SV40 transcriptional enhancer factor)