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Ontology Browser

Term:
Parent Terms Term With Siblings Child Terms
corneal disease +     
achromatopsia 4  
Achromatopsia 5  
Acrootoocular Syndrome 
Aicardi syndrome 
Alacrima +   
Albinism +   
aniridia +   
Arnold Stickler Bourne Syndrome 
ataxia with oculomotor apraxia type 3  
Ataxia-Microcephaly-Cataract Syndrome 
Ataxia-Oculomotor Apraxia 4  
basal laminar drusen  
bestrophinopathy  
Bothnia retinal dystrophy  
Bowman's membrane folds or rupture 
bradyopsia  
brittle cornea syndrome +   
cataract 17 multiple types  
cataract 22 multiple types  
cataract 35 
Cataract Microcornea Syndrome  
Cataract, Floriform 
Cataract, Pulverulent 
Cavitary Optic Disc Anomalies  
Cholestasis with Gallstone, Ataxia, and Visual Disturbance 
Choroideremia +   
Colobomatous Macrophthalmia with Microcornea 
cone-rod dystrophy +   
Congenital Alacrima +   
Congenital Fibrosis of Extraocular Muscles, 2  
Congenital Fibrosis of Extraocular Muscles, 3A, with or without Extraocular Involvement  
Congenital Fibrosis of Extraocular Muscles, 3B  
Congenital Fibrosis of Extraocular Muscles, 3C 
Congenital Fibrosis of Extraocular Muscles, 5  
Congenital Mydriasis +   
cornea cancer +  
cornea plana +   
Cornea Plana 1 
Cornea Plana 2  
corneal argyrosis 
corneal degeneration +   
corneal deposit +  
corneal dystrophy +   
Bilateral hereditary disorders of the cornea, usually autosomal dominant, which may be present at birth but more frequently develop during adolescence and progress slowly throughout life. Central macular dystrophy is transmitted as an autosomal recessive defect.
corneal ectasia 
corneal edema +   
Corneal Endothelial Cell Loss 
Corneal Graft Rejection  
Corneal Hypesthesia, Familial 
Corneal Injuries +   
corneal neovascularization +   
Corneal Opacity +   
corneal staphyloma 
Corneal Wavefront Aberration 
Dermoids of Cornea 
Duane retraction syndrome +   
enhanced S-cone syndrome  
Fleck Retina, Familial Benign  
Foveal Hypoplasia +   
Foveal Hypoplasia with Anterior Segment Anomalies  
Glaucoma 1, Open Angle, P  
Graves Ophthalmopathy  
Grouped Pigmentation of the Macula 
gyrate atrophy +   
hereditary night blindness +   
Hereditary Optic Atrophies +   
high hyperopia  
Histiocytic Dermatoarthritis 
Iris Pigment Epithelium Anomalies 
Joubert syndrome 8  
keratitis +   
keratoconus +   
keratopathy +  
Leber congenital amaurosis +   
Macular Dystrophy, X-Linked +   
megalocornea +   
Microcephaly and Chorioretinopathy +   
Microspherophakia +   
Neuhauser Syndrome 
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  
PORETTI-BOLTSHAUSER SYNDROME  
primary congenital glaucoma +   
pseudopapilledema 
pseudopterygium 
pterygium +   
Radial Drusen, Autosomal Dominant 
Ramos Arroyo Clark Syndrome 
renal hypomagnesemia 5 with ocular involvement  
Retinal Aplasia 
Retinal Dysplasia +   
Retinal Dystrophy, Early Onset Severe  
retinitis pigmentosa +   
Retinohepatoendocrinologic Syndrome 
Rhegmatogenous Retinal Detachment, Autosomal Dominant  
Ring Dermoid of Cornea  
sclerocornea +   
Spondyloocular Syndrome, Autosomal Recessive  
Stern Lubinsky Durrie Syndrome 
Stickler Syndrome, Type I, Nonsyndromic Ocular  
trachoma +   
Vascular Hyalinosis 
vitelliform macular dystrophy +   
Vitreoretinochoroidopathy  
Vitreoretinopathy with Phalangeal Epiphyseal Dysplasia  
Walker-Warburg syndrome +   
Weill-Marchesani syndrome +   

Synonyms
Exact Synonyms: CORNEAL DYSTROPHY, DOMINANT/RECESSIVE ;   Corneal Stromal Dystrophies ;   Corneal Stromal Dystrophy ;   Groenouw Dystrophies ;   Groenouw's Dystrophies ;   Groenouws Dystrophies ;   hereditary corneal dystrophies ;   hereditary corneal dystrophy
Narrow Synonyms: CORNEAL DYSTROPHY, DOMINANT ;   CORNEAL DYSTROPHY, RECESSIVE ;   Corneal Granular Dystrophies ;   Corneal Granular Dystrophy
Primary IDs: MESH:D003317
Alternate IDs: RDO:0000435
Xrefs: NCI:C34512 ;   NCI:C34513
Definition Sources: MESH:D003317

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