| COD/CORDs | Cone/cone-rod dystrophies |
| NGS | Next Generation Sequencing |
| SD-OCT | Spectral-Domain Optical Coherence Tomography |
| BAF/IRAF | Short-wave length /infra-red fundus autofluorescence |
| IRDs | Inherited retinal disorders |
| ERG | Electroretinogram |
| RCD | Rod-cone dystrophy |
| Ar | Autosomal recessive |
| Ad | Autosomal dominant |
| Xl | X-linked |
| ABCA4 | ATP-binding cassette, sub-family A, member 4 |
| GUCY2D | Guanylate Cyclase 2D |
| RPGR | Retinitis Pigmentosa GTPase regulator |
| SD | Standard deviation |
| BCVA | Best corrected visual acuity |
| ETDRS | Early Treatment Diabetic Retinopathy Study |
| RP | Retinitis Pigmentosa |
| MD | Macular Dystrophy |
| LCA | Leber Congenital Amaurosis |
| RPE | Retinal Pigment Epithelium |
| ELM | External limiting membrane |
| EZ | Ellipsoid zone |
| IZ | Interdigitation zone |
| HypoAF | Hypo-autofluorescence/hypo-autofluorescent |
| HyperAF | Hyper-autofluorescence/hyper-autofluorescent |