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GENATLAS PHENOTYPE

last update : 07-10-2016

Symbol	MCOP4
Location	8q22.1
Name	microphthalmia, isolated 4
Corresponding gene	GDF6
Main clinical features	heterogeneous group of ocular malformations with a more or less evident reduction in the size of the eyeball additional features include high hypermetropia and a short axial length, with size of the anterior chamber and the cornea in any cases reduced
Genetic determination	autosomal dominant
Function/system disorder	eye
Type	disease

Remark(s)