Monarch Disease Ontology term MONDO_0014982 (myopia 25, autosomal dominant) is 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; MYP25.