FG Syndrome Type 1FG syndrome 1FG syndrome caused by mutation in MED12MED12 FG syndromeOpitz-Kaveggia syndrome, X-linked recessiveFG syndromeFG syndrome type 1Keller syndromeOKSOpitz-Kaveggia syndromeintellectual disability, large head, imperforate anus, congenital hypotonia, and partial agenesis of corpus callosummental retardation, large head, imperforate anus, congenital hypotonia, and partial agenesis of corpus callosum
Definition
Any FG syndrome in which the cause of the disease is a mutation in the MED12 gene.
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