myopia Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description A refractive error characterized by the inability to see farther objects clearly. (Human Disease Ontology, DOID_11830)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0003100
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Genes

1 gene mutations causing the myopia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ADORA2A adenosine A2a receptor