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)
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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