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 +   
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 +   
A retrogressive pathological change in the retina, focal or generalized, caused by genetic defects, inflammation, trauma, vascular disease, or aging. Degeneration affecting predominantly the macula lutea of the retina is MACULAR DEGENERATION. (Newell, Ophthalmology: Principles and Concepts, 7th ed, p304)
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  

Synonyms
Exact Synonyms: Retinal Degenerations ;   degeneration of retina ;   retina degeneration
Narrow Synonyms: Autosomal dominant PRA ;   Generalized PRA ;   PRA ;   PRA 1 ;   PRA 2 ;   early retinal degeneration ;   progressive retinal atrophy
Primary IDs: MESH:D012162
Alternate IDs: OMIA:001297 ;   OMIA:001346 ;   OMIA:001521 ;   OMIA:001572 ;   OMIA:001984 ;   RDO:0001500
Definition Sources: MESH:D012162, https://en.wikipedia.org/wiki/Retinal_degeneration_(rhodopsin_mutation)

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