Myopia 25, autosomal dominant

MONDO:0014982

Any myopia (disease) in which the cause of the disease is a mutation in the P4HA2 gene.

Also known as: MYP25, P4HA2 myopia (disease), myopia (disease) caused by mutation in P4HA2, myopia 25, autosomal dominant, myopia 25, autosomal dominant; MYP25

10 clinical trials for this condition and its sub-types, 0 tagged with Myopia 25, autosomal dominant itself.

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↑ Myopia (274)

Including sub-types (10) Tagged with Myopia 25, autosomal dominant (0)

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