cleidocranial dysplasia (Q781618)

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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
  • Marie-Sainton Disease
  • cleidocranial dysostosis
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English
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
  • Marie-Sainton Disease
  • cleidocranial dysostosis

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