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Ontology Browser

Term:
Parent Terms Term With Siblings Child Terms
blindness +     
retinal disease +     
achromatopsia 4  
Achromatopsia 5  
Acrootoocular Syndrome 
Aicardi syndrome 
Al Gazali Sabrinathan Nair Syndrome 
Alacrima +   
Aland Island eye disease  
Albinism +   
Amaurosis Fugax  
angioid streaks +  
aniridia +   
ataxia with oculomotor apraxia type 3  
Ataxia with Oculomotor Apraxia Type 4  
Ataxia-Microcephaly-Cataract Syndrome 
Ausems Wittebol-Post Hennekam Syndrome 
basal laminar drusen  
bestrophinopathy  
Bietti crystalline corneoretinal dystrophy  
Bothnia retinal dystrophy  
bradyopsia  
cataract 17 multiple types  
cataract 22 multiple types  
cataract 35 
Cataract, Pulverulent 
Cavitary Optic Disc Anomalies  
Central Serous Chorioretinopathy  
Cholestasis with Gallstone, Ataxia, and Visual Disturbance 
chorioretinal scar +  
Choroideremia +   
color blindness +   
cone dystrophy +   
cone-rod dystrophy +   
Congenital Alacrima +   
congenital fibrosis of the extraocular muscles 1  
congenital fibrosis of the extraocular muscles 2  
congenital fibrosis of the extraocular muscles 3A  
congenital fibrosis of the extraocular muscles 3C 
congenital fibrosis of the extraocular muscles 5  
Congenital Mydriasis +   
Cornea Plana 1 
Cornea Plana 2  
corneal dystrophy +   
cortical blindness +   
Deaf-Blind Disorders +   
distal arthrogryposis type 5  
Duane retraction syndrome +   
enhanced S-cone syndrome  
exudative vitreoretinopathy +   
familial benign fleck retina  
Floriform Cataract 
FLOTCH Syndrome 
Foveal Hypoplasia +   
Foveal Hypoplasia with Anterior Segment Anomalies 
fundus albipunctatus  
Glaucoma 1, Open Angle, P  
Graves ophthalmopathy  
Grouped Pigmentation of the Macula 
gyrate atrophy +   
Hemianopsia 
hereditary night blindness +   
Hereditary Optic Atrophies +   
hereditary retinal dystrophy +   
High Hyperopia  
Histiocytic Dermatoarthritis 
hypertensive retinopathy  
Iris Hypoplasia and Glaucoma 
Iris Pigment Epithelium Anomalies 
Joubert syndrome 8  
Leber congenital amaurosis +   
megalocornea +   
Microcephaly and Chorioretinopathy +   
Microcephaly Microphthalmos Blindness 
Microcephaly with Chorioretinopathy, Autosomal Dominant 
neovascular inflammatory vitreoretinopathy  
nerve fibre bundle defect 
night blindness +   
Norrie disease  
Omphalocele, Diaphragmatic Hernia, and Radial Ray Defects 
Ophthalmomandibulomelic Dysplasia 
Peripapillary Atrophy, Beta Type 
Persistent Hyperplastic Primary Vitreous, Autosomal Dominant 
Persistent Hyperplastic Primary Vitreous, Autosomal Recessive  
pigmented paravenous chorioretinal atrophy  
Polycystic Kidney, Cataract, and Congenital Blindness 
PORETTI-BOLTSHAUSER SYNDROME  
primary congenital glaucoma +   
pseudopapilledema 
Radial Drusen, Autosomal Dominant 
Rambaud Galian Syndrome 
Ramos Arroyo Clark Syndrome 
renal hypomagnesemia 5 with ocular involvement  
Retina Reperfusion Injury  
Retinal Aplasia 
retinal arterial tortuosity  
retinal artery occlusion +   
retinal degeneration +   
retinal detachment +   
Retinal Dysplasia +   
retinal dystrophy with leukodystrophy  
Retinal Dystrophy, Early Onset Severe +   
retinal edema +   
Retinal Hemorrhage +   
Retinal Neoplasms +   
Retinal Neovascularization  
retinal perforation +  
retinal vascular disease +   
retinal vasculopathy with cerebral leukodystrophy  
retinitis +   
retinitis pigmentosa +   
Retinohepatoendocrinologic Syndrome 
retinopathy of prematurity +   
Rhegmatogenous Retinal Detachment, Autosomal Dominant  
Rodrigues Blindness 
Roifman Syndrome  
rubeosis iridis 
Scoliosis, Arachnodactyly, and Blindness 
Sickle Cell Retinopathy  
Spondyloocular Syndrome, Autosomal Recessive  
Stickler Syndrome, Type I, Nonsyndromic Ocular  
Vascular Hyalinosis 
visual impairment and progressive phthisis bulbi  
vitelliform macular dystrophy +   
Vitreoretinopathy with Phalangeal Epiphyseal Dysplasia  
Walker-Warburg syndrome +   
Webb-Dattani Syndrome  
Weill-Marchesani syndrome +   
X-Linked Macular Dystrophy +   
Yemenite Deaf-Blind Hypopigmentation Syndrome 

Synonyms
Exact Synonyms: Amaurosis Congenita
Primary IDs: MESH:C566720
Alternate IDs: OMIM:179900

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