Parietal Foramina with Cleidocranial Dysplasia, also known as cleidocranial dysplasia with parietal foramina,is related to cleidocranial dysplasia and night blindness, congenital stationary, 1b, autosomal recessive,and has symptoms including short clavicles, symmetrical, oval parietal bone defects and parietal foramina. An important gene associated with Parietal Foramina with Cleidocranial Dysplasia is MSX2 (Msh Homeobox 2), and among its related pathways is Mesenchymal Stem Cell Differentiation Pathways and Lineage-specific Markers. Affiliated tissues include bone

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