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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)