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Ontology Browser
Term:
Parent Terms Term With Siblings Child Terms
choroid disease +     
Hereditary Eye Diseases +     
achromatopsia 4  
Achromatopsia 5  
Acrootoocular Syndrome 
Aicardi syndrome  
Alacrima +   
Albinism +   
aniridia +   
ataxia with oculomotor apraxia type 3  
Ataxia-Microcephaly-Cataract Syndrome 
ataxia-oculomotor apraxia type 4  
autosomal dominant vitreoretinochoroidopathy  
basal laminar drusen  
bestrophinopathy  
Bothnia retinal dystrophy  
bradyopsia +   
cataract 17 multiple types  
cataract 22 multiple types  
cataract 35 
Cataract, Pulverulent 
Cavitary Optic Disc Anomalies  
Cholestasis with Gallstone, Ataxia, and Visual Disturbance 
Choroid Hemorrhage 
Choroid Neoplasms +   
Choroidal Effusions +  
Choroidal Neovascularization +   
choroidal sclerosis +   
Choroideremia +   
choroiditis +   
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 +   
Duane retraction syndrome +   
enhanced S-cone syndrome  
exudative vitreoretinopathy +   
familial benign fleck retina  
Floriform Cataract 
Foveal Hypoplasia +   
Foveal Hypoplasia with Anterior Segment Anomalies 
Glaucoma 1, Open Angle, P  
Graves ophthalmopathy  
Grouped Pigmentation of the Macula 
gyrate atrophy +   
Progressive, autosomal recessive, diffuse atrophy of the choroid, pigment epithelium, and sensory retina that begins in childhood.
hereditary night blindness +   
Hereditary Optic Atrophies +   
hereditary retinal dystrophy +   
High Hyperopia  
Histiocytic Dermatoarthritis 
Iris Pigment Epithelium Anomalies 
Joubert syndrome 8  
Leber congenital amaurosis +   
megalocornea +   
Microcephaly and Chorioretinopathy +   
Noble Bass Sherman 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  
Presumed Ocular Histoplasmosis Syndrome  
primary congenital glaucoma +   
pseudopapilledema 
Radial Drusen, Autosomal Dominant  
renal hypomagnesemia 5 with ocular involvement  
Retinal Aplasia 
Retinal Dysplasia +   
Retinal Dystrophy, Early Onset Severe +   
retinitis pigmentosa +   
Retinohepatoendocrinologic Syndrome 
Rhegmatogenous Retinal Detachment, Autosomal Dominant  
Spondyloocular Syndrome, Autosomal Recessive  
Stickler Syndrome, Type I, Nonsyndromic Ocular  
Vascular Hyalinosis 
vitelliform macular dystrophy +   
Vitreoretinopathy with Phalangeal Epiphyseal Dysplasia  
Walker-Warburg syndrome +   
Weill-Marchesani syndrome +   
X-Linked Macular Dystrophy +   

Synonyms
Exact Synonyms: GACR ;   Gyrate Atrophy of Choroid and Retina ;   Gyrate Atrophy of Choroid and Retina with Pyridoxine-Responsive Ornithinemia ;   Gyrate Atrophy of the Choroid and Retina ;   Gyrate atrophy of the choroid and/or retina ;   HOGA ;   Hyperornithinemia with Gyrate Atrophy of Choroid and Retina ;   OAT Deficiency ;   OKT Deficiency ;   Ornithine Aminotransferase Deficiency ;   Ornithine Delta Aminotransferase Deficiency ;   Ornithine Keto Acid Aminotransferase Deficiency ;   Ornithine Ketoacid Aminotransferase Deficiency ;   Ornithinemia with Gyrate Atrophy ;   gyrate atrophy of the retina
Primary IDs: MESH:D015799 ;   RDO:0001120
Alternate IDs: OMIM:258870
Xrefs: GARD:6556 ;   NCI:C84744
Definition Sources: MESH:D015799

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