| Gene | Associated with RETINAL DYSTROPHY WITH INNER RETINAL DYSFUNCTION AND GANGLION CELL ABNORMALITIES in | Link to HGNC | Cytogenetic band | Number of associated diseases | Associated diseases |
|---|---|---|---|---|---|
| ITM2B | ClinVar, OMIM, HUMSAVAR | HGNC link | 13q14.2 | 3 | 117300, 176500, 616079 |