Hearing Loss Disease Portal


 
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Most Common: Hearing Loss (D034381), Deafness (D003638), Sensorineural HL (D006319), Waardenburg Syndrome, Usher Syndromes
Disease Browser
Parent Node:
expandEye Diseases (D005128)
Parent Node:
expandRetinal Diseases (D012164)
..Starting node
..expandVitreoretinopathy, Proliferative (D018630)

       Child Nodes:
........expandExudative vitreoretinopathy 1 (C536382)
........expandEXUDATIVE VITREORETINOPATHY 2, X-LINKED (OMIM:305390)
........expandExudative Vitreoretinopathy 3 (C565297)
........expandExudative Vitreoretinopathy, Familial, X-Linked Recessive (C564428)
........expandVITREORETINOPATHY, NEOVASCULAR INFLAMMATORY (OMIM:193235)



 Sister Nodes: 
..expandAl Gazali Sabrinathan Nair syndrome (C535617)
..expandAngioid Streaks (D000793)
..expandAusems Wittebol-Post Hennekam syndrome (C538272)
..expandBestrophinopathy (C567518)
..expandBESTROPHINOPATHY, AUTOSOMAL RECESSIVE (OMIM:611809)
..expandBietti Crystalline Dystrophy (C535440)
..expandBothnia Retinal Dystrophy (C564392)
..expandCentral Serous Chorioretinopathy (D056833)
..expandCerebroretinal Microangiopathy with Calcifications and Cysts (C567401)
..expandDiabetic Retinopathy (D003930) Child1
..expandEpiretinal Membrane (D019773)
..expandExudative Vitreoretinopathy 4 (C566619)
..expandExudative Vitreoretinopathy 5 (C567648)
..expandFamilial Exudative Vitreoretinopathy (C580083)
..expandFleck Retina, Familial Benign (C565564)
..expandFLOTCH syndrome (C537065)
..expandFundus Albipunctatus (C562733)
..expandGrouped Pigmentation of the Macula (C565530)
..expandHypertensive Retinopathy (D058437)
..expandIris hypoplasia and glaucoma (C535538)
..expandLeber Congenital Amaurosis (D057130) Child20
..expandMicrocephaly with Chorioretinopathy, Autosomal Dominant (C563583)
..expandMicrocephaly with Chorioretinopathy, Autosomal Recessive (C565379)
..expandMICROPHTHALMIA, ISOLATED 5 (OMIM:611040)
..expandOculomelic amyoplasia (C537737)
..expandRambaud Galian syndrome (C535283)
..expandRamos Arroyo Clark syndrome (C535286)
..expandRetinal Aplasia (C566720)
..expandRetinal Artery Occlusion (D015356) Child1
..expandRetinal Degeneration (D012162) Child195
..expandRetinal Detachment (D012163) Child9
..expandRetinal Dysplasia (D015792) Child2
..expandRETINAL DYSPLASIA, PRIMARY (OMIM:312550)
..expandRetinal Hemorrhage (D012166) Child2
..expandRetinal Neoplasms (D019572) Child3
..expandRetinal Neovascularization (D015861)
..expandRetinal Nonattachment, Nonsyndromic Congenital (C565633)
..expandRetinal Perforations (D012167)
..expandRetinal Telangiectasis (D058456) Child1
..expandRetinal Vasculitis (D031300) Child1
..expandRetinal Vein Occlusion (D012170)
..expandRetinitis (D012173) Child4
..expandRetinopathy of Prematurity (D012178)
..expandRoifman syndrome (C535866)
..expandStickler Syndrome, Autosomal Recessive, COL9A1-Related (C565177)
..expandVasculopathy, Retinal, With Cerebral Leukodystrophy (C566007)
..expandVitreoretinopathy with Phalangeal Epiphyseal Dysplasia (C565179)
..expandVitreoretinopathy, Proliferative (D018630) Child5
   

Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM, CTD
Term ID:11645
Name:Vitreoretinopathy, Proliferative
Definition:Vitreoretinal membrane shrinkage or contraction secondary to the proliferation of primarily retinal pigment epithelial cells and glial cells, particularly fibrous astrocytes, followed by membrane formation. The formation of fibrillar collagen and cellular proliferation appear to be the basis for the contractile properties of the epiretinal and vitreous membranes.
Alternative IDs:
ParentIDs:MESH:D005128|MESH:D012164
TreeNumbers:C11.768.890 |C11.975
Synonyms:Inflammatories, Vitreoretinopathy Neovascular |Inflammatory, Vitreoretinopathy Neovascular |Neovascular Inflammatories, Vitreoretinopathy |Neovascular Inflammatory, Vitreoretinopathy |Proliferative Vitreoretinopathies |Proliferative Vitreoretinopathy |Vitreore
Slim Mappings:Eye disease
Reference: MedGen: D018630
MeSH: D018630
OMIM:

Genes:
Phenotypes
Disease Causing ClinVar Variants