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Summary Literature (0)
DOID:0111411 - exudative vitreoretinopathy 4

Disease Ontology Definition:An exudative vitreoretinopathy that has_material_basis_in homozygous, compound heterozygous, or heterozygous mutation in the LRP5 gene on chromosome 11q13.2.

Synonyms: EVR4

Xenbase Genes : lrp5


MIM:
MIM:601813 - EXUDATIVE VITREORETINOPATHY 4; EVR4

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view
Parent(s): autosomal genetic disease (is_a), exudative vitreoretinopathy (is_a)