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

0 clinical trials for this condition and its sub-types, 0 tagged with FG syndrome 1 itself.

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↑ FG syndrome (0) ↑ MED12-related intellectual disability syndrome (0)

Including sub-types (0) Tagged with FG syndrome 1 (0)

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