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GENATLAS PHENOTYPE

last update : 19/07/2006

Symbol	MCOP1
Location	14q32
Name	microphthalmia, isolated 1
Other name(s)	microphthalmos
Other symbol(s)	CMIC1
Main clinical features	congenital or associated with anterior segment abnormalities, partial or complete sclerocornea followed by corneal vascularisation and anterior staphyloma . associated with an elevated intraocular pressure
Genetic determination	autosomal recessive
Function/system disorder	eye
Type	disease