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Ontology Browser

Term:
persistent hyperplastic primary vitreous (DOID:0060282)
Annotations: Rat: (5) Mouse: (5) Human: (6) Chinchilla: (4) Bonobo: (5) Dog: (4) Squirrel: (4) Pig: (5)
Parent Terms Term With Siblings Child Terms
Eye Abnormalities +     
vitreous disease +     
3MC syndrome 1  
ablepharon macrostomia syndrome  
aniridia +   
Ankyloblepharon Filiforme Adnatum 
ankyloblepharon-ectodermal defects-cleft lip/palate syndrome  
Anophthalmia +   
anterior segment dysgenesis +   
Asymmetric Short Stature Syndrome 
Axenfeld-Rieger syndrome +   
Basel-Vanagaite-Smirin-Yosef syndrome  
blepharophimosis +   
Blue Diaper Syndrome 
Brachymetapody-Anodontia-Hypotrichosis-Albinoidism 
Brittle Cornea Syndrome +   
Chemke Oliver Mallek Syndrome 
Choroidal Effusions +  
chromosome 6pter-p24 deletion 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  
Diffuse Renal Mesangial Sclerosis, with Ocular Abnormalities 
Dwarfism Stiff Joint Ocular Abnormalities 
Ectopia Lentis +   
Egg-Shaped Pupil 
exudative vitreoretinopathy +   
FACES Syndrome 
Foveal Hypoplasia and Anterior Segment Dysgenesis  
Fronto-Facio-Nasal Dysplasia 
Frontoocular Syndrome 
Goniodysgenesis-Mental Retardation-Short Stature Syndrome 
hydrophthalmos +   
iridogoniodysgenesis syndrome +   
Joubert syndrome 1  
Joubert Syndrome 2  
Joubert syndrome 9  
Kapur Toriello Syndrome 
Maxillofacial Dysostosis 
Microcornea, Glaucoma, and Absent Frontal Sinuses 
Microcornea, Myopic Chorioretinal Atrophy, and Telecanthus  
microphthalmia +   
MOMES Syndrome 
neovascular inflammatory vitreoretinopathy  
Nephrotic Syndrome with Ocular Anomalies 
Neurodevelopmental Disorder with or without Anomalies of the Brain, Eye, or Heart  
oblique facial clefting 1  
oculoauricular syndrome  
Oculoauriculofrontonasal Syndrome 
Oculocerebrocutaneous Syndrome 
oculodentodigital dysplasia +   
Oculopalatocerebral Syndrome 
Oculorenocerebellar Syndrome 
Pena Shokeir Syndrome Type 2 
persistent hyperplastic primary vitreous +   
A developmental vitreous disease that is characterized by leukocoria, strabismus and vision loss, caused by failure of primary vitreous and hyaloid vasculature to regress during embryological development. (DO)
PHACE Association  
Pierson syndrome  
popliteal pterygium syndrome +   
Prepapillary Vascular Loops 
Pupillary Membrane, Persistence of 
Retinal Dysplasia +   
Rozin Hertz Goodman Syndrome 
Schmid-Fraccaro Syndrome  
Stromme syndrome  
torsion dystonia with onset in infancy  
vitreous abscess 
vitreous detachment +   
Vitreous Hemorrhage 
vitreous syneresis 

Synonyms
Exact Synonyms: Persistent Hyaloid Artery ;   persistent fetal vasculature syndrome ;   persistent hyaloid arteries ;   persistent hyaloid vasculature ;   persistent hyaloid vasculatures
Primary IDs: MESH:D054514
Xrefs: NCI:C161554 ;   OMIM:PS221900 ;   ORDO:91495
Definition Sources: https://en.wikipedia.org/wiki/Persistent_hyperplastic_primary_vitreous "DO"

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