Parietal foramina 1

MONDO:0008197

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, 0 tagged with Parietal foramina 1 itself.

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Including sub-types (1) Tagged with Parietal foramina 1 (0)

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