Eye Disorders

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Achromatopsia 2 - colorblindness
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Achromatopsia 3
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Albinism oculocutaneous type IA - OCA1A
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Albinism oculocutaneous type II - OCA2
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Albinism oculocutaneous type III - OCA3
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Albinism oculocutaneous type IV - OCA4
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Aniridia
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Arterial Calcification Generalized of Infancy - GACI1
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Axenfeld Rieger syndrome type 1 - RIEG1
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Axenfeld Rieger syndrome type 3 - RIEG3
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Basal laminar drusen
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Best macular dystrophy
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Cataract with late-onset corneal dystrophy
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Coloboma ocular
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Coloboma of optic nerve
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Cone-rod dystrophy 3
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Doyne Honeycomb degeneration of retina
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Ectopia lentis
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Enhanced S cone syndrome
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Foveal hyperplasia
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Gillespie syndrome
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Glaucoma 1 open angle E adult onset
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Glaucoma 1A primary open angle juvenile onset 1
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Glaucoma 3A primary open angle congenital juvenile or adult onset
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Hyperferritinemia-cataract syndrome
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Keratitis
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Leber congenital amaurosis 10 - LCA 10
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Leber congenital amaurosis 2
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Leber congenital amaurosis 8
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Leber hereditary optic neuropathy - LHON
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Macular degeneration juvenile
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Macular dystrophy patterned - Butterfly dystrophy of retinal pigment epithelium
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Microphthalmia syndromic 3
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Morning glory disc anomaly
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Night Blindness Congenital Statiionery Type 1E - CSNB1E
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Night blindness congenital stationary 1A X linked
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Night blindness congenital stationary 1B autosomal recessive
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Night blindness congenital stationary 1C autosomal recessive
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Night blindness congenital stationary 2A X linked
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Night blindness congenital stationary 2B autosomal recessive
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Ocular albinism type I - OA1
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Optic atrophy 1
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Optic atrophy 3 with cataract
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Optic nerve hypoplasia
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Optic nerve hypoplasia and abnormalities of the central nervous system
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Peters anomaly
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Pseudoxanthoma elasticum - PXE
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PXE-like disorder
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Retinitis pigmentosa
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Retinitis pigmentosa 12 autosomal recessive
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Retinitis pigmentosa 19
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Retinitis pigmentosa 2
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Retinitis pigmentosa 20
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Retinitis pigmentosa 25 - RP25
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Retinitis pigmentosa 3 - Retinitis pigmentosa 15 - Retinitis pigmentosa X linked
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Retinitis pigmentosa 37
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Retinitis pigmentosa 38 - RP38
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Retinitis pigmentosa 39 - RP39
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Retinitis pigmentosa 4 autosomal dominant or recessive
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Retinitis pigmentosa 40 - RP40
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Retinitis pigmentosa 43 - RP43
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Retinitis pigmentosa 7
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Retinoschisis - Retinoschisis X linked
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Stargardt disease 1
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Stargardt disease 3 - Stargardt like macular dystrophy
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Trichorhinophalangeal syndrome type I
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Trichorhinophalangeal syndrome type III
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TRP syndrome
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Vitreoretinochoroidopathy