Phenotypes for disease #03632 (MCOPCB11 (microphthalmia, syndromic, type 11 (MCOPCB-11)), OMIM:614402)

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Individual ID     
0000092997 bilateral severe microphthalmia, bilateral cleft lip and palate, developmental delays; 3.5y-growth parameters on 3rd centile, abnormal MRI with absent corpus callosum agenesis, cleft lip and palate - - Familial, autosomal recessive - - - - - Anne Slavotinek 00117527
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