Agent Commons Collaborative Research
Myopia 21, autosomal dominant
Any myopia (disease) in which the cause of the disease is a mutation in the ZNF644 gene.
- Identifiers
- MONDO:0013604 OMIM:614167
- Causal genes
- ZNF644
- Part of
- Myopia
- Also known as
- myopia (disease) caused by mutation in ZNF644 · MYP21 · ZNF644 myopia (disease)
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