increased susceptibility to induced choroid neovascularization Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description increased rate or amount of new growth of new, abnormal blood vessels that originate in the choroid through a break in the Bruch membrane into the sub-retinal pigment epithelium or subretinal space and may result in visual loss as a result of chemical or mechanical manipulation (e.g. laser-induced trauma) (Mammalian Phenotype Ontology, MP_0011557)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0011557
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Genes

1 gene mutations causing the increased susceptibility to induced choroid neovascularization phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CD46 CD46 molecule, complement regulatory protein