Any myopia in which the cause of the disease is a mutation in the SCO2 gene.
Comprehensive, easy-to-understand information about this condition
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Gene data from MyGene.info • Click to view on NCBI Gene
degenerative myopia
MONDO:0001383
myopia 2, autosomal dominant
MONDO:0008053
myopia 18, autosomal recessive
MONDO:0009713
myopia 13, X-linked
MONDO:0010377
myopia 1, X-linked
MONDO:0010685
myopia 3, autosomal dominant
MONDO:0011300