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Summary Literature (0)
MIM:614292 - MYOPIA, HIGH, WITH CATARACT AND VITREORETINAL DEGENERATION; MCVD

Xenbase Genes: p3h2

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0013670 - myopia, high, with cataract and vitreoretinal degeneration
MONDO:0020207 - obsolete rare isolated myopia