decreased visual acuity Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description Visual impairment (or vision impairment) is vision loss (of a person) to such a degree as to qualify as an additional support need through a significant limitation of visual capability resulting from either disease, trauma, or congenital or degenerative conditions that cannot be corrected by conventional means, such as refractive correction, medication, or surgery. (Human Phenotype Ontology, HP_0000505)
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4 gene mutations causing the decreased visual acuity phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CFH complement factor H
CHRNB2 cholinergic receptor, nicotinic, beta 2 (neuronal)
OTX2 orthodenticle homeobox 2
PDE6B phosphodiesterase 6B, cGMP-specific, rod, beta