Send us a Message
Submit Data |  Help |  Video Tutorials |  News |  Publications |  Download |  REST API |  Citing RGD |  Contact   
Search RGD Grant Resources Citing RGD About Us Contact Us
Genes Variants Community Projects QTLs Strains Markers Genome Information Ontologies Cell Lines References Download Submit Data
OntoMate (Literature Search) JBrowse (Genome Browser) Synteny Browser (VCMap) Variant Visualizer Multi-Ontology Enrichment (MOET) Gene-Ortholog Location Finder (GOLF) InterViewer (Protein-Protein Interactions) PhenoMiner (Quatitative Phenotypes) Gene Annotator OLGA (Gene List Generator) AllianceMine GViewer (Genome Viewer)
Aging & Age-Related Disease Cancer & Neoplastic Disease Cardiovascular Disease Coronavirus Disease Developmental Disease Diabetes Hematologic Disease Immune & Inflammatory Disease Infectious Disease Liver Disease Neurological Disease Obesity & Metabolic Syndrome Renal Disease Respiratory Disease Sensory Organ Disease
Find Models   new Genetic Models Autism Models Rat PhenoMiner (Quantitative Phenotypes) Chinchilla PhenoMiner Expected Ranges (Quantitative Phenotype) PhenoMiner Term Comparison Hybrid Rat Diversity Panel Phenotypes Phenotypes in Other Animal Models Animal Husbandry Strain Medical Records Phylogenetics Strain Availability Calendar Rats 101 Submissions Photo Archive
Pathways
Rat Community Forum Directory of Rat Laboratories Video Tutorials News RGD Publications RGD Presentations Archive Nomenclature Guidelines Resource Links Laboratory Resources Employment Resources

Ontology Browser
Term:
Parent Terms Term With Siblings Child Terms
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 Neovascularization +   
cone dystrophy +   
corneal neovascularization +   
distal arthrogryposis type 5  
Eales Disease  
enhanced S-cone syndrome  
familial benign fleck retina  
FLOTCH Syndrome 
foveal hypoplasia 1  
foveal hypoplasia 2  
fundus albipunctatus  
Grouped Pigmentation of the Macula 
hypertensive retinopathy  
Iris Hypoplasia and Glaucoma 
Leber congenital amaurosis +   
Microcephaly and Chorioretinopathy +   
Microcephaly with Chorioretinopathy, Autosomal Dominant 
neovascular inflammatory vitreoretinopathy  
nerve fibre bundle defect 
night blindness +   
Ocular Neovascularization +   
Rambaud Galian Syndrome 
Ramos Arroyo Clark Syndrome 
Retina Reperfusion Injury  
Retinal Aplasia 
retinal arterial tortuosity  
retinal artery occlusion +   
retinal degeneration +   
retinal detachment +   
Retinal Dysplasia +   
retinal dystrophy with leukodystrophy  
retinal edema +   
Retinal Hemorrhage +   
Retinal Neoplasms +   
Retinal Neovascularization  
Formation of new blood vessels originating from the retinal veins and extending along the inner (vitreal) surface of the retina.
retinal perforation +  
retinal vascular disease +   
retinal vasculopathy with cerebral leukodystrophy  
retinitis +   
retinopathy of prematurity +   
Roifman Syndrome  
rubeosis iridis 
Sickle Cell Retinopathy  
Vitreoretinopathy with Phalangeal Epiphyseal Dysplasia  

Synonyms
Primary IDs: MESH:D015861 ;   RDO:0006930
Definition Sources: MESH:D015861

paths to the root