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