Eye diseases | Page 3

572 diseases found in 6 pages

G Diseases

GM1 gangliosidosis type 3 GMS syndrome Goldberg-Shprintzen megacolon syndrome Goldenhar disease Goldmann-Favre syndrome Graham-Cox syndrome Griscelli syndrome type 1 Griscelli syndrome type 2 Griscelli syndrome type 3 Groenouw type I corneal dystrophy Gyrate atrophy of choroid and retina

H Diseases

Hallermann-Streiff syndrome Hereditary endotheliopathy, retinopathy, nephropathy, and stroke Hereditary hemorrhagic telangiectasia Hereditary hemorrhagic telangiectasia type 2 Hereditary hemorrhagic telangiectasia type 3 Hereditary hemorrhagic telangiectasia type 4 Hereditary vascular retinopathy Hermansky Pudlak syndrome 2 Homocystinuria due to CBS deficiency Horizontal gaze palsy with progressive scoliosis Hurler–Scheie syndrome Hurler syndrome Hyperferritinemia cataract syndrome Hypohidrotic ectodermal dysplasia autosomal recessive Hypomelanosis of Ito Hypomyelination and congenital cataract Hypoparathyroidism familial isolated

I Diseases

Ichthyosis lamellar 1 Ichthyosis lamellar, autosomal dominant Incontinentia pigmenti Infantile cerebellar retinal degeneration Intraocular melanoma IRVAN syndrome Isolated congenital megalocornea Isolated ectopia lentis

J Diseases

Jacobsen syndrome Joubert syndrome with oculorenal anomalies Junctional epidermolysis bullosa, Herlitz type Juvenile polyposis syndrome Juvenile retinoschisis

K Diseases

Kabuki syndrome Kaufman oculocerebrofacial syndrome Kearns-Sayre syndrome Keratitis, hereditary Keratoconjunctivitis sicca Keratoconus Keratosis follicularis spinulosa decalvans KID syndrome Knobloch syndrome Krabbe disease Kyphoscoliotic Ehlers-Danlos syndrome

L Diseases

Lacrimo-auriculo-dento-digital syndrome Lamellar ichthyosis Landau-Kleffner syndrome Laryngoonychocutaneous syndrome Late-onset retinal degeneration Lattice corneal dystrophy type 1 Lattice corneal dystrophy type 3A Laurence-Moon syndrome LCHAD deficiency Leber congenital amaurosis Leber congenital amaurosis 1 Leber congenital amaurosis 10 Leber congenital amaurosis 11 Leber congenital amaurosis 12 Leber congenital amaurosis 13 Leber congenital amaurosis 14 Leber congenital amaurosis 15 Leber congenital amaurosis 16 Leber congenital amaurosis 2 Leber congenital amaurosis 3 Leber congenital amaurosis 4 Leber congenital amaurosis 6 Leber congenital amaurosis 9 Leber hereditary optic neuropathy Leber hereditary optic neuropathy with dystonia Leigh syndrome, French Canadian type Lenz microphthalmia syndrome LEOPARD syndrome Leukodystrophy Ligneous conjunctivitis Limb-mammary syndrome Linear nevus sebaceous syndrome Lowe oculocerebrorenal syndrome Lowry Maclean syndrome Lubinsky syndrome Lymphedema-distichiasis syndrome

M Diseases

Macrosomia with lethal microphthalmia Macular dystrophy, corneal type 1 Macular telangiectasia type 2 Marfan syndrome Marinesco-Sjogren syndrome Marshall syndrome Martsolf syndrome Maternally inherited diabetes and deafness Meckel syndrome Meesmann corneal dystrophy Megalocornea-intellectual disability syndrome Megalocornea - spherophakia - secondary glaucoma

The RareGuru disease database is regularly updated using data generously provided by GARD, the United States Genetic and Rare Disease Information Center.

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