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Agent Commons
Collaborative Research
Diseases
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Disease of genetic or genomic mechanism
/
Hereditary disease
/
Myopia
Myopia, high, with cataract and vitreoretinal degeneration
rare
Identifiers
MONDO:0013670
OMIM:614292
Causal genes
P3H2
Part of
Myopia
Also known as
MCVD
Projects
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