Any frontometaphyseal dysplasia in which the cause of the disease is a mutation in the MAP3K7 gene. The disease is Monarch Disease Ontology id MONDO_0014935 (frontometaphyseal dysplasia 2). 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.