Home Page
References OMIM Gene GeneReviews HGMD HGNC
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