Retinal Hamartoma Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A hamartoma (a benign, focal malformation consisting of a disorganized mixture of cells and tissues) of the retina. (Human Phenotype Ontology, HP_0009594)
External Link https://www.disgenet.org/browser/0/1/0/C1863411
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Genes

4 genes associated with the disease Retinal Hamartoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
AKT1 v-akt murine thymoma viral oncogene homolog 1
PTEN phosphatase and tensin homolog
TSC1 tuberous sclerosis 1
TSC2 tuberous sclerosis 2