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parietal foramina 1

Disease Summary
Associated Targets (2)
Tbio

2


Mondo Description Any parietal foramina in which the cause of the disease is a mutation in the MSX2 gene.
Uniprot Description Autosomal dominant disease characterized by oval defects of the parietal bones caused by deficient ossification around the parietal notch, which is normally obliterated during the fifth fetal month.
Mondo Term and Equivalent IDs
MONDO:0008197:  parietal foramina 1