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GENATLAS PHENOTYPE
last update : 23-09-2010
Symbol MCOP2
Location 14q23.1
Name microphthalmia, isolated 2
Corresponding gene VSX2 , OTX2
Main clinical features
  • bilateral profound microphthalmia without associated anomalies and with normal intelligence
  • Genetic determination autosomal recessive
    Function/system disorder eye
    Type disease
    Remark(s)