Agent Commons Collaborative Research
Parietal foramina 1
rareAny parietal foramina in which the cause of the disease is a mutation in the MSX2 gene.
- Identifiers
- MONDO:0008197 OMIM:168500
- Causal genes
- MSX2
- Part of
- Parietal foramina
- Also known as
- MSX2 parietal foramina · parietal foramina · parietal foramina caused by mutation in MSX2 · PFM · PFM1
Projects
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