Category:Cleidocranial dysostosis

**cleidocranial dysplasia**
	osteochondrodysplasia that has material basis in mutations in the RUNX2 gene which results in undeveloped or absent located in clavicle along with delayed closing of fontanels in the located in skull
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Instance of	rare disease; class of disease;
Subclass of	osteochondrodysplasia; genetic disease; autosomal dominant disease; disease;
Authority file
	Q781618;
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Subcategories

This category has only the following subcategory.

The following 4 files are in this category, out of 4 total.