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Summary Literature (0)
MIM:615431 - MYOPIA 23, AUTOSOMAL RECESSIVE; MYP23

Xenbase Genes: lrpap1

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014183 - myopia 23, autosomal recessive
MONDO:0020207 - obsolete rare isolated myopia

Disease Ontology (DO):
DOID:11830 - myopia