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Ontology Browser
Term:
Parent Terms Term With Siblings Child Terms
Eye Abnormalities +     
Vascular Malformations +     
3MC syndrome 1  
ablepharon macrostomia syndrome  
aniridia +   
Ankyloblepharon Filiforme Adnatum  
ankyloblepharon-ectodermal defects-cleft lip/palate syndrome  
Anophthalmia +   
anterior segment dysgenesis +   
arterial tortuosity syndrome  
Arterio-Arterial Fistula +  
arteriovenous malformation +   
Asymmetric Short Stature Syndrome 
Axenfeld-Rieger syndrome +   
Basel-Vanagaite-Smirin-Yosef syndrome  
blepharophimosis +   
Blue Diaper Syndrome 
Brachymetapody-Anodontia-Hypotrichosis-Albinoidism 
Brittle Cornea Syndrome +   
Central Nervous System Vascular Malformations +   
Chemke Oliver Mallek Syndrome 
Choroidal Effusions +  
chromosome 6pter-p24 deletion syndrome 
CLOVES syndrome  
CODAS syndrome  
Cole-Carpenter syndrome +   
coloboma +   
Colobomatous Macrophthalmia with Microcornea 
Congenital Nephrotic Syndrome with or without Ocular Abnormalities +   
Craniofacial Anomalies and Anterior Segment Dysgenesis Syndrome  
Craniosynostosis with Ocular Abnormalities and Hallucal Defects 
cryptophthalmia +   
De Hauwere syndrome  
DeSanto-Shinawi syndrome  
Developmental Delay, Language Impairment, and Ocular Abnormalities  
Distichiasis with Congenital Anomalies of the Heart and Peripheral Vasculature 
Duane-radial ray syndrome  
Dwarfism Stiff Joint Ocular Abnormalities 
Ectopia Lentis +   
Egg-Shaped Pupil 
exudative vitreoretinopathy +   
FACES Syndrome 
familial multiple nevi flammei  
foveal hypoplasia 2  
Fronto-Facio-Nasal Dysplasia 
Frontoocular Syndrome 
Goniodysgenesis-Mental Retardation-Short Stature Syndrome 
Hemophilia A with Vascular Abnormality 
hereditary hemorrhagic telangiectasia +   
hydrophthalmos +   
intellectual developmental disorder with ocular anomalies and distinctive facial features  
iridogoniodysgenesis syndrome +   
Joubert syndrome 1  
Joubert Syndrome 2  
Joubert syndrome 9  
Kapur Toriello Syndrome  
Maxillofacial Dysostosis 
May-Thurner Syndrome 
Meningioangiomatosis 
Microcephaly-Capillary Malformation Syndrome  
Microcornea, Glaucoma, and Absent Frontal Sinuses 
Microcornea, Myopic Chorioretinal Atrophy, and Telecanthus  
microphthalmia +   
MOMES Syndrome 
MYELOFIBROSIS, CONGENITAL, WITH ANEMIA, NEUTROPENIA, DEVELOPMENTAL DELAY, AND  
Nephrotic Syndrome with Ocular Anomalies 
neurodevelopmental disorder with eye movement abnormalities and ataxia  
NEURODEVELOPMENTAL DISORDER WITH INTENTION TREMOR, PYRAMIDAL SIGNS, DYSPRAXIA, AND OCULAR ANOMALIES  
Neurodevelopmental Disorder with or without Anomalies of the Brain, Eye, or Heart  
NEURODEVELOPMENTAL DISORDER WITH SPEECH DELAY AND VARIABLE OCULAR ANOMALIES  
NEUROOCULAR SYNDROME 1  
NEUROOCULAR SYNDROME 2, PAROXYSMAL TYPE  
oblique facial clefting 1  
oculoauricular syndrome  
Oculoauriculofrontonasal Syndrome 
Oculocerebrocutaneous Syndrome 
oculodentodigital dysplasia +   
OCULOGASTROINTESTINAL NEURODEVELOPMENTAL SYNDROME  
Oculopalatocerebral Syndrome 
Oculorenocerebellar Syndrome 
Patent Ductus Venosus  
Pena Shokeir Syndrome Type 2 
Persistence of Pupillary Membrane 
persistent hyperplastic primary vitreous +   
PHACE Association  
Pierson syndrome  
popliteal pterygium syndrome +   
Prepapillary Vascular Loops 
Primary Intraosseous Vascular Malformation  
Pulmonary Atresia +   
retinal arterial tortuosity  
Retinal Dysplasia +   
Rozin Hertz Goodman Syndrome 
Schmid-Fraccaro Syndrome  
scimitar syndrome +   
SHORT STATURE, IMPAIRED INTELLECTUAL DEVELOPMENT, MICROCEPHALY, HYPOTONIA, AND OCULAR ANOMALIES  
Single Umbilical Artery 
Splenoportal Vascular Anomalies 
Stromme syndrome  
torsion dystonia with onset in infancy  
Vascular Fistula +   

Synonyms
Exact Synonyms: Preretinal Vascular Loops
Primary IDs: MESH:C563287
Alternate IDs: MIM:264060

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