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Cleidocranial Dysplasia — Gene Therapy & Clinical Trials | FollowGene
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Cleidocranial Dysplasia
Cleidocranial Dysplasia
Prevalence:
1/1000000
skeletal
Official
·
OMIM:119600
Official
·
ORPHA1452
Clavicle and skull developmental disorder due to RUNX2 gene mutations.
Associated Genes
RUNX2
RUNX Family Transcription Factor 2
Chromosome 6
Autosomal Dominant