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Ontology Browser

Term:
exudative vitreoretinopathy 4 (DOID:0111411)
Annotations: Rat: (1) Mouse: (1) Human: (1) Chinchilla: (1) Bonobo: (1) Dog: (1) Squirrel: (1) Pig: (1)
Parent Terms Term With Siblings Child Terms
Aicardi-Goutieres syndrome +   
autosomal dominant disease +   
autosomal hemophilia A 
autosomal recessive disease +   
blepharophimosis, ptosis, and epicanthus inversus syndrome  
camptodactyly-tall stature-scoliosis-hearing loss syndrome  
congenital nystagmus 1  
exudative vitreoretinopathy 1  
exudative vitreoretinopathy 3 
exudative vitreoretinopathy 4  
An exudative vitreoretinopathy that has_material_basis_in homozygous, compound heterozygous, or heterozygous mutation in LRP5 on chromosome 11q13.2. (DO)
exudative vitreoretinopathy 5  
exudative vitreoretinopathy 6  
exudative vitreoretinopathy 7  
factor XI deficiency  
familial adenomatous polyposis +   
familial Mediterranean fever +   
Gillespie syndrome  
hypophosphatasia +   
McCune Albright syndrome  
progeria +   
Robinow syndrome +   
septooptic dysplasia +   
syndromic microphthalmia 12  
syndromic microphthalmia 14  
syndromic microphthalmia 8  
thrombophilia due to thrombomodulin defect  
Weill-Marchesani syndrome +   
X-linked exudative vitreoretinopathy 2  

Synonyms
Exact Synonyms: EVR4
Narrow Synonyms: exudative vitreoretinopathy 4, autosomal dominant ;   exudative vitreoretinopathy 4, autosomal recessive ;   exudative vitreoretinopathy 4, digenic
Primary IDs: MESH:C566619
Alternate IDs: OMIM:601813
Definition Sources: https://www.ncbi.nlm.nih.gov/pubmed/15024691 "DO"

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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.