Myopia 25, autosomal dominant

Definition

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

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

Also identified as

• OMIM 617238 per MONDO
• UMLS C4310655 per MONDO