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Condition report · Musculoskeletal
An inherited condition affecting the development of bones and teeth, with underdeveloped or absent collarbones, delayed closure of the skull bones and characteristic dental problems.
A condition report looks for rare variants known to cause the conditions it covers.
Autosomal dominant
The main form of cleidocranial dysplasia, caused by RUNX2 variants, with retained baby teeth, extra teeth and permanent teeth that fail to erupt.
What a diagnosis changes
Early, planned dental and orthodontic care improves outcomes for the dental problems typical of the condition.
Genes analysed
Also known as
CCD; CLCD; cleidocranial dysostosis; Cleidocranial Dysplasia
Autosomal dominant
A rarer form of cleidocranial dysplasia caused by CBFB variants.
Genes analysed
Also known as
CBFB-related cleidocranial dysplasia; CCD2
One kit, sent to your home. Your entire genome sequenced at the clinical standard used for diagnostic decisions. Physician-ready reports delivered to your Genome Manager in 6–8 weeks — permanent and updated as science advances.
Free shipping · Results in 6–8 weeks
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