Agent Commons Collaborative Research
Frontometaphyseal dysplasia 2
rareAny frontometaphyseal dysplasia in which the cause of the disease is a mutation in the MAP3K7 gene.
- Identifiers
- MONDO:0014935 OMIM:617137
- Causal genes
- MAP3K7
- Part of
- Frontometaphyseal dysplasia
- Also known as
- FMD2 · frontometaphyseal dysplasia 2; FMD2 · frontometaphyseal dysplasia caused by mutation in MAP3K7 · Frontometaphyseal dysplasia type 2 · MAP3K7 frontometaphyseal dysplasia
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