Myopia 21, autosomal dominant

MONDO:0013604

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

Also known as: ZNF644 myopia (disease), myopia (disease) caused by mutation in ZNF644, myopia 21, autosomal dominant, MYP21

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

Follow this condition — get notified about new trials

Broader categories

Sort by