Specific

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

General

chronic eye disease (chronic ophthalmopathy) genetic disease