achromatic retinal patches Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Areas of the retina lacking pigmentation. (Human Phenotype Ontology, HP_0009727)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0009727
Similar Terms
Downloads & Tools

Genes

2 genes associated with the achromatic retinal patches phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
TSC1 tuberous sclerosis 1
TSC2 tuberous sclerosis 2