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Ontology Browser

Parent Terms Term With Siblings Child Terms
angioid streaks of choroid 
Bietti crystalline corneoretinal dystrophy  
Choroideremia +   
Encephalopathy with Intracranial Calcification, Growth Hormone Deficiency, Microcephaly, and Retinal Degeneration 
enhanced S-cone syndrome  
fundus dystrophy +   
hereditary spastic paraplegia 15  
High Myopia with Cataract and Vitreoretinal Degeneration  
Hyaloideoretinal Degeneration of Wagner  
infantile cerebellar-retinal degeneration  
Joubert syndrome 4  
late-onset retinal degeneration  
Lattice Degeneration of Retina Leading to Retinal Detachment 
MacKay Shek Carr Syndrome 
macular degeneration +   
Microphthalmia with Hyperopia, Retinal Degeneration, Macrophakia, and Dental Anomalies 
Noble Bass Sherman Syndrome 
peripheral retinal degeneration +  
pigmented paravenous chorioretinal atrophy  
Retinal Cone Dystrophy 1 
Retinal Degeneration and Epilepsy 
Retinal Degeneration, Autosomal Recessive, Clumped Pigment Type  
retinal drusen +   
retinitis pigmentosa +   
retinoschisis +   
A vitreoretinal dystrophy characterized by splitting of the neuroretinal layers. It occurs in two forms: degenerative retinoschisis and X chromosome-linked juvenile retinoschisis.
Senior-Loken Syndrome 7  
snowflake vitreoretinal degeneration  
Sveinsson chorioretinal atrophy  

Exact Synonyms: Degenerative Retinoschises ;   Degenerative Retinoschisis ;   Juvenile Retinoschises ;   Juvenile Retinoschisis ;   RS ;   Retinoschises
Primary IDs: MESH:D041441
Alternate IDs: RDO:0004341
Xrefs: ICD10CM:H33.10 ;   ICD9CM:361.10 ;   NCI:C85046
Definition Sources: MESH:D041441

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