Myopia 25, autosomal dominant

Any myopia (disease) in which the cause of the disease is a mutation in the P4HA2 gene.

Also known as: MYP25, P4HA2 myopia (disease), myopia (disease) caused by mutation in P4HA2, myopia 25, autosomal dominant, myopia 25, autosomal dominant; MYP25

16 clinical trials for this condition and its sub-types.