chorioretinal dysplasia Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Abnormal development of the choroid and retina. (Human Phenotype Ontology, HP_0007731)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0007731
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Genes

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

Symbol Name
KIF11 kinesin family member 11