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Ontology Browser

Term:
Parent Terms Term With Siblings Child Terms
bestrophinopathy  
Concentric Annular Macular Dystrophy  
congenital hypotrichosis with juvenile macular dystrophy  
degeneration of macula and posterior pole +   
diabetic maculopathy +   
ectodermal dysplasia, ectrodactyly, and macular dystrophy syndrome  
Geographic Atrophy  
Kuhnt-Junius degeneration +   
Macular Degeneration, Early-Onset  
Macular Dystrophy with Central Cone Involvement  
Macular Dystrophy, Fenestrated Sheen Type 
macular retinal edema +   
Myoclonic Epilepsy, Congenital Deafness, Macular Dystrophy, and Psychiatric Disorders 
occult macular dystrophy  
A macular degeneration that is characterized by a central cone dysfunction leading to a loss of vision with a normal fundus and normal fluorescein angiography findings. (DO)
patterned macular dystrophy +   
retinal macular dystrophy +   
Sorsby's fundus dystrophy  
Stargardt Macular Degeneration Absent or Hypoplastic Corpus Callosum Mental Retardation and Dysmorphic Features 
vitelliform macular dystrophy +   
X-Linked Macular Dystrophy +   

Synonyms
Exact Synonyms: OCMD ;   OMD
Broad Synonyms: RP1L1-RELATED CONDITION
Primary IDs: MIM:613587 ;   RDO:0009914
Definition Sources: http://www.iovs.org/content/41/2/513.full.pdf "DO" "DO"

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