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GENATLAS PHENOTYPE
last update : 01-10-2013
Symbol MYP23
Location 4p16.3
Name myopia 23
Corresponding gene LRPAP1
Main clinical features
  • nonsyndromic extreme myopia with spherical equivalents of -17 diopters or greater and subnormal best-corrected visual acuity
  • Genetic determination autosomal recessive
    Function/system disorder eye
    Type disease
    Remark(s)