NIH/National Eye Institute
About NIH/National Eye Institute
The National Eye Institute (NEI) was established by Congress in 1968 to protect and prolong the vision of the American people. NEI research leads to sight-saving treatments, reduces visual impairment and blindness, and improves the quality of life for people of all ages. NEI-supported research has advanced our knowledge of how the visual system functions in health and disease. Vision research is supported by the NEI through approximately 1600 research grants and training awards made to scientists at more than 250 medical centers, hospitals, universities, and other institutions across the country and around the world. The NEI also conducts laboratory and patient-oriented research at its own facilities located on the NIH campus in Bethesda, Maryland.
Related Rare Diseases:
- Neuropathic Ocular Pain
- Neurotrophic Keratitis
- COL4A1/A2-Related Disorders
- X-linked Retinoschisis
- Hyperferritinemia Cataract Syndrome
- Congenital Fibrosis of the Extraocular Muscles
- Megalocornea Intellectual Disability Syndrome
- Congenital Varicella Syndrome
- Ablepharon-Macrostomia Syndrome
- Oculocerebral Syndrome with Hypopigmentation
- Schwartz Jampel Syndrome
- Lenz Microphthalmia Syndrome
- Nance-Horan Syndrome
- Aniridia Cerebellar Ataxia Mental Deficiency
- Mulibrey Nanism
- WAGR Syndrome/11p Deletion Syndrome
- Vogt-Koyanagi-Harada Disease
- Chromosome 18q- Syndrome
- Senior-Løken Syndrome
- Chromosome 18 Ring
- Chandler’s Syndrome
- SHORT Syndrome
- Chromosome 6 Ring
- Weill Marchesani Syndrome
- Keratitis Ichthyosis Deafness Syndrome
- Marshall Syndrome
- Alström Syndrome
- Horner’s Syndrome
- Eales Disease
- Axenfeld-Rieger Syndrome
- Coats Disease
- Marcus Gunn Phenomenon
- Adie Syndrome
- Keratomalacia
- Papillitis
- Rothmund-Thomson Syndrome
- Wyburn-Mason Syndrome
- Keratoconus
- Norrie Disease
- Vernal Keratonconjunctivitis
- Leber Hereditary Optic Neuropathy
- Usher Syndrome
- Choroideremia
- Isolated Aniridia
- Retinoschisis
- Posterior Uveitis
- Neuromyelitis Optica Spectrum Disorder
- Pars Planitis
- Corneal Dystrophies
- Waardenburg Syndrome
- Stickler Syndrome
- Crouzon Syndrome
- PLA2G6-Associated Neurodegeneration
- Conradi Hünermann Syndrome
- Oculo-Auriculo-Vertebral Spectrum
- Best Vitelliform Macular Dystrophy
- Macular Degeneration
- Leber Congenital Amaurosis
- Retinoblastoma
- Cogan-Reese Syndrome
- Pseudoxanthoma Elasticum
- Retinopathy of Prematurity
- Duane syndrome
- Cytomegalovirus Infection
- Von Hippel-Lindau Disease
- Brown Syndrome
- Essential Iris Atrophy
- Retinitis Pigmentosa
- Sjögren Syndrome
- Behçet’s Syndrome
- Nanismo de Mulibrey
- Síndrome de Behçet
- Síndrome de Crouzon
- Síndrome de Senior-Løken
- Síndrome de Rothmund-Thomson
- Coroideremia
- Síndrome de Usher
- Síndrome SHORT
- Síndrome de abléfaron-macrostomía
- Síndrome oculocerebral con hipopigmentación
- TRPM3-Related Neurodevelopmental Disorder
