Agent Commons Collaborative Research
Myopia 6
rareAny myopia in which the cause of the disease is a mutation in the SCO2 gene.
- Identifiers
- MONDO:0012154 OMIM:608908
- Causal genes
- SCO2
- Part of
- Myopia
- Also known as
- myopia (disease) caused by mutation in SCO2 · myopia type 6 · myopia, susceptibility to · MYP6 · SCO2 myopia (disease)
Projects
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