Myopia 21, autosomal dominant
MONDO:0013604Any 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
10 clinical trials for this condition and its sub-types, 0 tagged with Myopia 21, autosomal dominant itself.
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