Eye diseases | Page 6

572 diseases found in 6 pages

S Diseases

Slow-channel congenital myasthenic syndrome Smith-Lemli-Opitz syndrome Snowflake vitreoretinal degeneration Sotos syndrome Spastic paraplegia 2 Spastic paraplegia 7 Spastic tetraplegia-retinitis pigmentosa-intellectual disability syndrome Spinocerebellar ataxia 7 Spinocerebellar ataxia autosomal recessive 5 Spinocerebellar degeneration and corneal dystrophy Spondyloepiphyseal dysplasia SRD5A3-CDG (CDG-Iq) Stargardt disease Sturge-Weber syndrome Subaortic stenosis short stature syndrome Superior limbic keratoconjunctivitis Syndromic microphthalmia, type 3

T Diseases

Tangier disease Tay-Sachs disease Tietz syndrome Tolosa Hunt syndrome Trachoma Treacher Collins syndrome Triple A syndrome Triploidy Trisomy 13 Trisomy 18 Tuberous sclerosis Tubulointerstitial nephritis and uveitis Tucker syndrome Tyrosinemia type 2

U Diseases

Usher syndrome Usher syndrome, type 1 Usher syndrome, type 1B Usher syndrome, type 1C Usher syndrome, type 1D Usher syndrome, type 1E Usher syndrome, type 1F Usher syndrome type 2A Usher syndrome, type 2B Usher syndrome, type 2C Usher syndrome type 3A Uveal diseases

V Diseases

Verloes Van Maldergem Marneffe syndrome Vernal keratoconjunctivitis Vici syndrome Visual snow syndrome Vogt-Koyanagi-Harada disease Von Hippel-Lindau disease

W Diseases

Waardenburg syndrome type 1 Waardenburg syndrome type 2 Waardenburg syndrome type 3 Waardenburg syndrome type 4 Wagner syndrome WAGR syndrome Walker-Warburg syndrome Weill-Marchesani syndrome Werner syndrome Williams syndrome Wilson disease Wolf-Hirschhorn syndrome Wolfram syndrome Wrinkly skin syndrome Wyburn-Mason syndrome

X Diseases

X-linked Charcot-Marie-Tooth disease type 5 X-linked congenital generalized hypertrichosis X-linked congenital stationary night blindness X-linked dominant chondrodysplasia punctata 2 X-linked hypohidrotic ectodermal dysplasia X-linked ichthyosis X-linked myotubular myopathy

Z Diseases

Zellweger syndrome

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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