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Ontology Browser

Term:
Parent Terms Term With Siblings Child Terms
retinal disease +     
Al Gazali Sabrinathan Nair Syndrome 
angioid streaks +  
Ausems Wittebol-Post Hennekam Syndrome 
bestrophinopathy  
Bietti crystalline corneoretinal dystrophy  
Bothnia retinal dystrophy  
bradyopsia  
Central Serous Chorioretinopathy  
chorioretinal scar +  
cone dystrophy +   
A retinal disease that is characterized by the loss of cone cells, the photoreceptors responsible for both central and color vision. (DO)
enhanced S-cone syndrome  
Fleck Retina, Familial Benign  
FLOTCH Syndrome 
fundus albipunctatus  
Grouped Pigmentation of the Macula 
hypertensive retinopathy  
Iris Hypoplasia and Glaucoma  
Leber congenital amaurosis +   
Microcephaly and Chorioretinopathy +   
Microcephaly with Chorioretinopathy, Autosomal Dominant 
nerve fibre bundle defect 
night blindness +   
Oculomelic Amyoplasia  
preretinal fibrosis  
proliferative vitreoretinopathy +   
Rambaud Galian Syndrome 
Ramos Arroyo Clark Syndrome 
Retina Reperfusion Injury  
Retinal Aplasia 
Retinal Arterial Macroaneurysm with Supravalvular Pulmonic Stenosis  
Retinal Arteries, Tortuosity of  
retinal artery occlusion +   
retinal degeneration +   
retinal detachment +   
Retinal Dysplasia +   
retinal edema +   
Retinal Hemorrhage +   
Retinal Neoplasms +   
Retinal Neovascularization  
retinal perforation +  
retinal vascular disease +   
retinal vasculitis +   
Retinal Vasculopathy with Cerebral Leukodystrophy  
retinitis +   
retinopathy of prematurity +   
Roifman Syndrome  
rubeosis iridis 
Sickle Cell Retinopathy  
Vitreoretinopathy with Phalangeal Epiphyseal Dysplasia  

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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.