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Myopia 25, autosomal dominant
Any myopia (disease) in which the cause of the disease is a mutation in the P4HA2 gene.
This condition has no sub-types.
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Explore conditions, clinical trials, and the organisations running them.
Up to: Myopia
Any myopia (disease) in which the cause of the disease is a mutation in the P4HA2 gene.
This condition has no sub-types.