retinal disease
eye disease that is located in the retina
cone dystrophy
inherited ocular disorder characterized by the loss of cone cells
white dot syndrome
eye disease
macular hole
small break in the macula, located in the center of the eye's light-sensitive tissue called the retina
retinal haemorrhage
symptom
night blindness
condition making it difficult or impossible to see in relatively low light
retinal vascular disease
Retinal damage resulting from diminished blood flow/oxygenation due to abnormalities of the retinal vessels. Causes include hypertension, diabetes, thrombosis, embolism, and hemorrhage.
iris hypoplasia with glaucoma
human disease
retinitis
Human disease
enhanced S-cone syndrome
Goldmann-Favre syndrome (GFS) is a vitreoretinal dystrophy characterized by early onset of night blindness, reduced bilateral visual acuity, and typical fundus findings (progressive pigmentary degenerative changes, macular edema, retinoschisis)
Leber congenital amaurosis
retinal disease that is characterized by nystagmus, sluggish or no pupillary responses, and severe vision loss or blindness
retinal degeneration
retinal disease that is characterized by deterioration of the retina caused by the progressive and eventual death of the cells of the retina
Retinal dysplasia
eye disease
retinal detachment
human disease