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Ontology Browser

Term:
Parent Terms Term With Siblings Child Terms
retinal disease +     
absolute glaucoma 
Al Gazali Sabrinathan Nair Syndrome 
Aland Island eye disease  
angioid streaks +  
Ausems Wittebol-Post Hennekam Syndrome 
bestrophinopathy  
Bietti crystalline corneoretinal dystrophy  
bradyopsia  
Central Serous Chorioretinopathy  
chorioretinal scar +  
choroidal sclerosis +   
cone dystrophy +   
conjunctival degeneration +  
corneal degeneration +   
degenerative myopia  
distal arthrogryposis type 5  
enhanced S-cone syndrome  
familial benign fleck retina  
FLOTCH Syndrome 
fundus albipunctatus  
Grouped Pigmentation of the Macula 
hypertensive retinopathy  
Iris Hypoplasia and Glaucoma 
Leber congenital amaurosis +   
leukocoria 
Microcephaly and Chorioretinopathy +   
Microcephaly with Chorioretinopathy, Autosomal Dominant 
neovascular inflammatory vitreoretinopathy  
nerve fibre bundle defect 
night blindness +   
Rambaud Galian Syndrome 
Ramos Arroyo Clark Syndrome 
Retina Reperfusion Injury  
Retinal Aplasia 
retinal arterial tortuosity  
retinal artery occlusion +   
retinal degeneration +   
A retinal disease that is characterized by deterioration of the retina caused by the progressive and eventual death of the cells of the retina. (DO)
retinal detachment +   
Retinal Dysplasia +   
retinal dystrophy with leukodystrophy  
retinal edema +   
Retinal Hemorrhage +   
Retinal Neoplasms +   
Retinal Neovascularization  
retinal perforation +  
retinal vascular disease +   
retinal vasculopathy with cerebral leukodystrophy  
retinitis +   
retinopathy of prematurity +   
Roifman Syndrome  
rubeosis iridis 
Sickle Cell Retinopathy  
siderosis of eye 
snowflake vitreoretinal degeneration  
Vitreoretinopathy with Phalangeal Epiphyseal Dysplasia  
vitreous syneresis 

Synonyms
Exact Synonyms: degeneration of retina ;   retina degeneration ;   retinal degenerations
Narrow Synonyms: PRA ;   PRA 1 ;   PRA 2 ;   autosomal dominant PRA ;   early retinal degeneration ;   generalized PRA ;   progressive retinal atrophy
Primary IDs: MESH:D012162
Alternate IDs: OMIA:001297 ;   OMIA:001346 ;   OMIA:001521 ;   OMIA:001572 ;   OMIA:001984
Xrefs: NCI:C34979
Definition Sources: https://en.wikipedia.org/wiki/Retinal_degeneration_(rhodopsin_mutation) "DO" "DO"

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