Parietal foramina 1

Any parietal foramina in which the cause of the disease is a mutation in the MSX2 gene.

Also known as: MSX2 parietal foramina, parietal foramina 1, parietal foramina caused by mutation in MSX2, PFM, PFM1, catlin Marks, cranium bifidum occultum, cranium bifidum, hereditary

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