FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term exudative vitreoretinopathy 4 ID (Ontology) DOID:0111411 (Human Disease)
Definition An exudative vitreoretinopathy that has_material_basis_in homozygous, compound heterozygous, or heterozygous mutation in the LRP5 gene on chromosome 11q13.2.
Also Known As "EVR4"
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DO.org
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 Genes
 exudative vitreoretinopathy 4       2
 for disease ribbon | exudative vitreoretinopathy 4       2
 model of | exudative vitreoretinopathy 4       2
Spanning Tree (Parents/Children)
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monogenic disease
 |__autosomal genetic disease____
retinal vascular disease         |
 |__exudative vitreoretinopathy__|
                                 exudative vitreoretinopathy 4  2 rec.
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Is a exudative vitreoretinopathy
autosomal genetic disease
Part of
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Synonyms
  • "EVR4" EXACT OMO:0003012
Secondary IDs
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MESH:C566619
MIM:601813