Frontometaphyseal dysplasia 2

Any frontometaphyseal dysplasia in which the cause of the disease is a mutation in the MAP3K7 gene.

Also known as: FMD2, Frontometaphyseal dysplasia 2, Frontometaphyseal dysplasia type 2, MAP3K7 frontometaphyseal dysplasia, frontometaphyseal dysplasia 2; FMD2, frontometaphyseal dysplasia caused by mutation in MAP3K7

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