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Ontology Browser
Term:
Parent Terms Term With Siblings Child Terms
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  
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 
Choroideremia +   
Concentric Annular Macular 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 hypotrichosis with juvenile macular dystrophy  
Congenital Mydriasis +   
Cornea Plana 1 
Cornea Plana 2  
corneal dystrophy +   
degeneration of macula and posterior pole +   
diabetic maculopathy +  
Duane retraction syndrome +   
ectodermal dysplasia, ectrodactyly, and macular dystrophy syndrome  
enhanced S-cone syndrome  
exudative vitreoretinopathy +   
familial benign fleck retina  
Floriform Cataract 
Foveal Hypoplasia +   
Foveal Hypoplasia with Anterior Segment Anomalies 
Geographic Atrophy  
Glaucoma 1, Open Angle, P  
Graves ophthalmopathy  
Grouped Pigmentation of the Macula 
gyrate atrophy +   
hereditary night blindness +   
Hereditary Optic Atrophies +   
hereditary retinal dystrophy +   
High Hyperopia  
Histiocytic Dermatoarthritis 
Iris Pigment Epithelium Anomalies 
Joubert syndrome 8  
Kuhnt-Junius degeneration +   
Leber congenital amaurosis +   
Macular Degeneration, Early-Onset  
Macular Dystrophy with Central Cone Involvement  
Macular Dystrophy, Fenestrated Sheen Type 
macular retinal edema +   
megalocornea +   
Microcephaly and Chorioretinopathy +   
Myoclonic Epilepsy, Congenital Deafness, Macular Dystrophy, and Psychiatric Disorders 
occult macular dystrophy  
Omphalocele, Diaphragmatic Hernia, and Radial Ray Defects 
Ophthalmomandibulomelic Dysplasia 
patterned macular dystrophy +   
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 
Radial Drusen, Autosomal Dominant  
renal hypomagnesemia 5 with ocular involvement  
Retinal Aplasia 
Retinal Dysplasia +   
Retinal Dystrophy, Early Onset Severe +   
retinal macular dystrophy +   
retinitis pigmentosa +   
Retinohepatoendocrinologic Syndrome 
Rhegmatogenous Retinal Detachment, Autosomal Dominant  
Sorsby's fundus dystrophy  
Spondyloocular Syndrome, Autosomal Recessive  
Stargardt Macular Degeneration Absent or Hypoplastic Corpus Callosum Mental Retardation and Dysmorphic Features 
Stickler Syndrome, Type I, Nonsyndromic Ocular  
Vascular Hyalinosis 
vitelliform macular dystrophy +   
A macular degeneration that it is characterized by the disruption of cells in a small area near the center of the retina, the macula and may cause progressive vision loss. (DO)
Vitreoretinopathy with Phalangeal Epiphyseal Dysplasia  
Walker-Warburg syndrome +   
Weill-Marchesani syndrome +   
X-Linked Macular Dystrophy +   

Synonyms
Exact Synonyms: vitelliform dystrophy ;   vitelliform macular dystrophies
Primary IDs: MESH:D057826
Xrefs: GARD:10120 ;   NCI:C118788 ;   OMIM:PS153840 ;   ORDO:1243 ;   ORDO:99000
Definition Sources: http://en.wikipedia.org/wiki/Vitelliform_macular_dystrophy "DO" "DO", http://ghr.nlm.nih.gov/condition/vitelliform-macular-dystrophy "DO" "DO"

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