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Ontology Browser
Term:
Parent Terms Term With Siblings Child Terms
fundus dystrophy +     
retinal disease +     
Al Gazali Sabrinathan Nair Syndrome 
Aland Island eye disease  
angioid streaks +  
Ausems Wittebol-Post Hennekam Syndrome 
bestrophinopathy  
Bietti crystalline corneoretinal dystrophy  
Bothnia retinal dystrophy  
Boucher-Neuhauser syndrome  
bradyopsia +   
Central Serous Chorioretinopathy  
chorioretinal scar +  
cone dystrophy +   
cone-rod dystrophy +   
distal arthrogryposis type 5  
dominant pericentral pigmentary retinopathy 
dystrophies primarily involving the retinal pigment epithelium +   
enhanced S-cone syndrome  
familial benign fleck retina  
FLOTCH Syndrome 
foveal hypoplasia 1  
foveal hypoplasia 2  
fundus albipunctatus  
A fundus dystrophy that is characterized by discrete uniform white dots over the entire fundus with greatest density in the midperiphery and no macular involvement. (DO)
Ghose Sachdev Kumar Syndrome 
Grouped Pigmentation of the Macula 
hereditary retinal dystrophy +   
hypertensive retinopathy  
Iris Hypoplasia and Glaucoma 
Leber congenital amaurosis +   
Microcephaly and Chorioretinopathy +   
Microcephaly with Chorioretinopathy, Autosomal Dominant 
Myoectodermal Gonadal Dysgenesis Syndrome  
neovascular inflammatory vitreoretinopathy  
nerve fibre bundle defect 
night blindness +   
Pseudoinflammatory Fundus Dystrophy, Finnish Type  
Rambaud Galian Syndrome 
Ramos Arroyo Clark Syndrome 
Reticular Dystrophy of Retinal Pigment Epithelium  
Reticular Pigmentary Retinal Dystrophy of Posterior Pole 
Retina Reperfusion Injury  
Retinal Aplasia 
retinal arterial tortuosity  
retinal artery occlusion +   
retinal degeneration +   
retinal detachment +   
Retinal Dysplasia +   
retinal dystrophies primarily involving Bruch's membrane 
RETINAL DYSTROPHY AND IRIS COLOBOMA WITH OR WITHOUT CONGENITAL CATARACT  
Retinal Dystrophy and Microvillus Inclusion Disease  
Retinal Dystrophy and Obesity  
retinal dystrophy in systemic or cerebroretinal lipidoses 
RETINAL DYSTROPHY WITH INNER RETINAL DYSFUNCTION AND GANGLION CELL ABNORMALITIES  
retinal dystrophy with leukodystrophy  
RETINAL DYSTROPHY WITH OR WITHOUT EXTRAOCULAR ANOMALIES  
Retinal Dystrophy with or without Macular Staphyloma  
Retinal Dystrophy, Early Onset Severe +   
Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome  
Retinal Dystrophy, Juvenile Cataracts, and Short Stature Syndrome  
Retinal Dystrophy, Optic Nerve Edema, Splenomegaly, Anhidrosis, and Migraine Headache Syndrome  
retinal edema +   
Retinal Hemorrhage +   
Retinal Neoplasms +   
Retinal Neovascularization  
retinal perforation +   
retinal vascular disease +   
retinal vasculopathy with cerebral leukodystrophy  
retinitis +   
retinitis pigmentosa +   
retinopathy of prematurity +   
Roifman Syndrome  
rubeosis iridis 
Sickle Cell Retinopathy  
vitreoretinal dystrophy 
Vitreoretinopathy with Phalangeal Epiphyseal Dysplasia  

Synonyms
Exact Synonyms: pigmentary retinal dystrophy
Narrow Synonyms: FUNDUS ALBIPUNCTATUS, AUTOSOMAL RECESSIVE ;   RETINITIS PUNCTATA ALBESCENS ;   RETINITIS PUNCTATA ALBESCENS, AUTOSOMAL DOMINANT
Primary IDs: MESH:C562733
Alternate IDs: MIM:136880
Definition Sources: http://www.omim.org/entry/136880 "DO" "DO"

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