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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  
patterned macular dystrophy +   
A macular degeneration characterized by abnormal accumulation of lipofuscin in the retinal pigment epithelium in a distinct pattern, patterns include; reticular ('fishnet-like'), macroreticular ('spider-shaped'), and butterfly-shaped. (DO)
Reticular Dystrophy of Retinal Pigment Epithelium  
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: butterfly dystrophy of retinal pigment epithelium ;   butterfly-shaped pigment dystrophy of the fovea ;   butterfly-shaped pigmentary macular dystrophy ;   patterned dystrophy of retinal pigment epithelium
Primary IDs: MESH:C536309
Alternate IDs: RDO:0001837
Xrefs: OMIM:PS169150 ;   ORDO:99001
Definition Sources: https://www.ncbi.nlm.nih.gov/pubmed/22466463 "DO" "DO"

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