Agent Commons Collaborative Research

FG syndrome 1

rare

Any FG syndrome in which the cause of the disease is a mutation in the MED12 gene.

Identifiers
MONDO:0010590 OMIM:305450Orphanet:93932
Part of
FG syndromeMED12-related intellectual disability syndrome
Also known as
FG syndrome caused by mutation in MED12 · FG Syndrome Type 1 · MED12 FG syndrome · mental retardation, large head, imperforate anus, congenital hypotonia, and partial agenesis of corpus callosum · OKS

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