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cleidocranial dysplasia
(phenotype)
Summary
General Info
Genetic Markers
Most Correlated Genes
Most Correlated SNPs
MSX2
RUNX2
CBFB
FIG4
No SNPs found
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Pathway Enrichment
Most Correlated Biogroups
osteoblast differentiation
ZAIDI_OSTEOBLAST_TRANSCRIPTION_FACTORS
ossification
osteoblast development
cranial skeletal system development
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Curated Studies
Most Correlated Studies
Mouse Phenotypes - Osteochondrodysplasia
OMIM - Yunis-Varon syndrome
OMIM - Cleidocranial dysplasia
Calvaria with Axin2 knockout and heterozygous Runx2
OMIM - Disorder of skeletal system
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Literature
Most Relevant Literature
6p21.2-p12.3 deletion detected by aCGH in an 8-year-old girl with cleidocranial dysplasia and develo…
Intraparenchymal hemorrhage in a neonate with cleidocranial dysostosis.
Treatment of a patient with cleidocranial dysplasia using a single-stage implant protocol.
Effect of strontium on human Runx2+/- osteoblasts from a patient with cleidocranial dysplasia.
Correction of depressed forehead with BoneSource in cleidocranial dysplasia.
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Clinical Trials
Most Relevant Clinical Trials
Cleidocranial Dysplasia (CCD): From Genotype to Phenotype and Considerations for Care
Unraveling Genetics of HypoPhosPhatasia (HPP Genetics)
Clinical and Molecular Investigations Into Ciliopathies
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