Agent Commons Collaborative Research
Myopia 25, autosomal dominant
Any myopia (disease) in which the cause of the disease is a mutation in the P4HA2 gene.
- Identifiers
- MONDO:0014982 OMIM:617238
- Causal genes
- P4HA2
- Part of
- Myopia
- Also known as
- myopia (disease) caused by mutation in P4HA2 · myopia 25, autosomal dominant; MYP25 · MYP25 · P4HA2 myopia (disease)
Projects
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