genetic disease of the eye
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More general terms
More specific terms
- achromatopsia (colorblindness)
- Aland island eye disease (Forsius-Eriksson type ocular albinism)
- aniridia
- anophthalmia (microphthalmia 2)
- anterior segment mesenchymal dysgenesis (anterior segment ocular dysgenesis)
- autosomal dominant keratitis
- Avellino corneal dystrophy
- Behr's disease
- bestrophinopathy
- bilateral optic nerve hypoplasia/aplasia
- bull's eye maculopathy (concentric annular macular dystrophy)
- cataract-microcornea syndrome
- central areolar choroidal dystrophy
- choroidal atrophy (vitreoretinochoroidopathy)
- choroidal dystrophy
- choroideremia; progressive choroidal atrophy; progressive tapetochoroidal dystrophy
- Cockayne syndrome
- cone-rod dystrophy (CORD)
- congenital night blindness
- congenital stromal corneal dystrophy (CSCD)
- corneal dystrophy & perceptive deafness; corneal dystrophy & sensorineural deafness; Harboyan syndrome
- corneal dystrophy Fuchs endothelial type
- corneal dystrophy Groenouw type 1; corneal dystrophy granular type
- corneal dystrophy lattice type 1
- corneal dystrophy of Bowman layer type 1; Reis-Buecklers corneal dystrophy
- corneal dystrophy of Bowman layer type 2; corneal dystrophy Thiel-Behnke type
- corneal endothelial dystrophy; Chandler syndrome
- corneal fleck dystrophy
- Doyne honeycomb retinaldystrophy (DHRD); malattia leventinese (MLVT)
- ectopia pupillae
- enhanced S cone syndrome (ESCS); Goldmann-Favre syndrome; retinoschisis with early hemeralopia
- epithelial basement membrane corneal dystrophy; Cogan corneal dystrophy; map-dot-fingerprint type corneal dystrophy
- exfoliation syndrome (exfoliation glaucoma)
- familial cataracts
- familial exudative vitreoretinopathy (FEVR); Criswick-Schepens syndrome
- familial myopia
- foveal hypoplasia
- fundus albipunctatus
- fundus flavimaculatus
- gelatinous drop-like corneal dystrophy; lattice corneal dystrophy type 3
- hypomagnesemia renal with ocular involvement
- iridogoniodysgenesis anomaly
- lattice corneal dystrophy type 3A
- Leber congenital amaurosis
- Leber hereditary optic neuropathy (Leber optic atrophy, LHON)
- Leber optic atrophy & dystonia; familial dystonia with visual failure & striatal lucencies
- macular corneal dystrophy
- Meesmann corneal dystrophy; epithelial corneal dystrophy
- microphthalmia (nanophthalmos)
- microspherophakia
- ocular albinism with late-onset sensorineural deafness (OASD)
- oculocutaneous albinism
- open-angle glaucoma (OAG)
- optic atrophy 1 (Kyer-type optic atrophy)
- osteoporosis pseudoglioma syndrome; osteogenesis imperfecta ocular form
- patterned dystrophy of retinal pigment epithelium
- pericentral retinal dystrophy
- Peters anomaly
- pigmented paravenous chorioretinal atrophy (PPCRA)
- posterior polymorphous corneal dystrophy
- primary congenital glaucoma
- retinal cone dystrophy
- retinitis pigmentosa (RP)
- retinitis punctata albescens
- retinol-binding protein deficiency
- rhegmatogenous retinal detachment autosomal dominant
- ring dermoid of cornea
- Sorsby fundus dystrophy
- Stargardt disease
- susceptibility to diabetic nephropathy; susceptibility to microvascular complications of diabetes type 7 (MVCD7); susceptibility to diabetic proliferative retinopathy
- Sveinsson chorioretinal atrophy; atrophia areata; helicoidal peripapillary chorioretinal degeneration
- Usher syndrome
- vitelliform macular dystrophy; Best macular dystrophy