Myopia 21, autosomal dominant

Definition

Any myopia (disease) in which the cause of the disease is a mutation in the ZNF644 gene.

Also known as myopia (disease) caused by mutation in ZNF644, myopia 21, autosomal dominant, ZNF644 myopia (disease) — per MONDO

Also identified as

• OMIM 614167 per MONDO
• UMLS C3279997 per MONDO