| Dataset | HPO Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| External Link | http://compbio.charite.de/hpoweb/showterm?id=HP:0001105 |
| Similar Terms | |
| Downloads & Tools |
8 genes associated with the retinal atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
| Symbol | Name |
|---|---|
| CTSD | cathepsin D |
| LAMA1 | laminin, alpha 1 |
| MERTK | MER proto-oncogene, tyrosine kinase |
| POMGNT1 | protein O-linked mannose N-acetylglucosaminyltransferase 1 (beta 1,2-) |
| POMT1 | protein-O-mannosyltransferase 1 |
| RBP4 | retinol binding protein 4, plasma |
| RS1 | retinoschisin 1 |
| SLC7A14 | solute carrier family 7, member 14 |
