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 QTLs Strains Markers Genome Information Ontologies Cell Lines References Download Submit Data
OntoMate (Literature Search) JBrowse (Genome Browser) Variant Visualizer Multi-Ontology Enrichment (MOET) Gene-Ortholog Location Finder (GOLF) InterViewer (Protein-Protein Interactions) PhenoMiner (Quatitative Phenotypes) Gene Annotator OLGA (Gene List Generator) RatMine GViewer (Genome Viewer) Overgo Probe Designer ACP Haplotyper VCMap
Aging & Age-Related Disease Cancer Cardiovascular Disease COVID-19 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 PhenoMiner (Quantitative Phenotypes) Expected Ranges (Quantitative Phenotype) PhenoMiner Term Comparison Hybrid Rat Diversity Panel Phenotypes GERRC (Gene Editing Rat Resource Center) 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 Poster Archive Nomenclature Guidelines Resource Links Laboratory Resources Employment Resources

Ontology Browser
Term:
Parent Terms Term With Siblings Child Terms
retinal detachment +     
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 +   
distal arthrogryposis type 5  
Diverticulosis of Bowel, Hernia, and Retinal Detachment 
enhanced S-cone syndrome  
familial benign fleck retina  
FLOTCH Syndrome 
fundus albipunctatus  
Grouped Pigmentation of the Macula 
hypertensive retinopathy  
Iris Hypoplasia and Glaucoma 
Knobloch Syndrome  
Knobloch Syndrome Type II 
Knobloch Syndrome Type III 
Lattice Degeneration of Retina Leading to Retinal Detachment 
Leber congenital amaurosis +   
Microcephaly and Chorioretinopathy +   
Microcephaly with Chorioretinopathy, Autosomal Dominant 
neovascular inflammatory vitreoretinopathy  
nerve fibre bundle defect 
night blindness +   
Persistent Hyperplastic Primary Vitreous, Autosomal Recessive  
preretinal fibrosis  
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  
retinal perforation +  
Perforations through the whole thickness of the retina including the macula as the result of inflammation, trauma, degeneration, etc. The concept includes retinal breaks, tears, dialyses, and holes.
retinal vascular disease +   
retinal vasculitis +   
retinal vasculopathy with cerebral leukodystrophy  
retinitis +   
retinopathy of prematurity +   
Rhegmatogenous Retinal Detachment, Autosomal Dominant  
Roifman Syndrome  
rubeosis iridis 
Sickle Cell Retinopathy  
Spondyloocular Syndrome, Autosomal Recessive  
Vitreoretinopathy with Phalangeal Epiphyseal Dysplasia  

Synonyms
Exact Synonyms: Retinal Break ;   Retinal Dialyse ;   Retinal Dialyses ;   Retinal Hole ;   Retinal Holes ;   Retinal Perforations ;   Retinal Tear ;   Retinal dialysis ;   retinal breaks ;   retinal tears
Primary IDs: MESH:D012167
Alternate IDs: RDO:0006479
Xrefs: NCI:C50732

paths to the root