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Cleidocranial Dysplasia Index

Featured: Cleidocranial Dysplasia Main Article
Cleidocranial dysplasia is a genetic condition. Cleidocranial dysplasia is also referred to as cleidocranial dysostosis and cleidocranial dysostosis. Cleidocranial dysplasia primarily affects bone and teeth development. Symptoms and signs may vary widely with severity. The RUNX2 is the gene that is related to cleidocranial dysplasia. Cleidocranial dysplasia is an autosomal dominant pattern inherited condition.

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Terms related to Cleidocranial Dysplasia:

  • Cleidocranial Dysostosis
  • Marie-Sainton Syndrome
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