FG syndrome 1

MONDO:0010590

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

Also known as: FG Syndrome Type 1, FG syndrome 1, FG syndrome caused by mutation in MED12, MED12 FG syndrome, Opitz-Kaveggia syndrome, X-linked recessive, FG syndrome, FG syndrome type 1, Keller syndrome

28 clinical trials for this condition and its sub-types.

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