|Dataset||MPO Gene-Phenotype Associations|
|Category||disease or phenotype associations|
|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)|
|Downloads & Tools|
1 gene mutations causing the increased susceptibility to induced choroid neovascularization phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
|CD46||CD46 molecule, complement regulatory protein|