Eye Disorders

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

Achromatopsia 2 - colorblindness

Achromatopsia 3

Albinism oculocutaneous type IA - OCA1A

Albinism oculocutaneous type II - OCA2

Albinism oculocutaneous type III - OCA3

Albinism oculocutaneous type IV - OCA4

Aniridia

Arterial Calcification Generalized of Infancy - GACI1

Axenfeld Rieger syndrome type 1 - RIEG1

Axenfeld Rieger syndrome type 3 - RIEG3

Basal laminar drusen

Best macular dystrophy

Cataract with late-onset corneal dystrophy

Coloboma ocular

Coloboma of optic nerve

Cone-rod dystrophy 3

Doyne Honeycomb degeneration of retina

Ectopia lentis

Enhanced S cone syndrome

Foveal hyperplasia

Gillespie syndrome

Glaucoma 1 open angle E adult onset

Glaucoma 1A primary open angle juvenile onset 1

Glaucoma 3A primary open angle congenital juvenile or adult onset

Hyperferritinemia-cataract syndrome

Keratitis

Leber congenital amaurosis 10 - LCA 10

Leber congenital amaurosis 2

Leber congenital amaurosis 8

Leber hereditary optic neuropathy - LHON

Macular degeneration juvenile

Macular dystrophy patterned - Butterfly dystrophy of retinal pigment epithelium

Microphthalmia syndromic 3

Morning glory disc anomaly

Night Blindness Congenital Statiionery Type 1E - CSNB1E

Night blindness congenital stationary 1A X linked

Night blindness congenital stationary 1B autosomal recessive

Night blindness congenital stationary 1C autosomal recessive

Night blindness congenital stationary 2A X linked

Night blindness congenital stationary 2B autosomal recessive

Ocular albinism type I - OA1

Optic atrophy 1

Optic atrophy 3 with cataract

Optic nerve hypoplasia

Optic nerve hypoplasia and abnormalities of the central nervous system

Peters anomaly

Pseudoxanthoma elasticum - PXE

PXE-like disorder

Retinitis pigmentosa

Retinitis pigmentosa 12 autosomal recessive

Retinitis pigmentosa 19

Retinitis pigmentosa 2

Retinitis pigmentosa 20

Retinitis pigmentosa 25 - RP25

Retinitis pigmentosa 3 - Retinitis pigmentosa 15 - Retinitis pigmentosa X linked

Retinitis pigmentosa 37

Retinitis pigmentosa 38 - RP38

Retinitis pigmentosa 39 - RP39

Retinitis pigmentosa 4 autosomal dominant or recessive

Retinitis pigmentosa 40 - RP40

Retinitis pigmentosa 43 - RP43

Retinitis pigmentosa 7

Retinoschisis - Retinoschisis X linked

Stargardt disease 1

Stargardt disease 3 - Stargardt like macular dystrophy

Trichorhinophalangeal syndrome type I

Trichorhinophalangeal syndrome type III

TRP syndrome

Vitreoretinochoroidopathy