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

1 clinical trial for this condition and its sub-types.