exudative retinopathy Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description OMIM mapping confirmed by DO. [SN]. (Human Disease Ontology, DOID_7765)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0007898
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Genes

3 genes associated with the exudative retinopathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
CTC1 CTS telomere maintenance complex component 1
NDP Norrie disease (pseudoglioma)
TINF2 TERF1 (TRF1)-interacting nuclear factor 2