Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0020497
Disease: Cortical Congenital Hyperostosis
Cortical Congenital Hyperostosis
0.010 Biomarker disease BEFREE CMO is a clinical equivalent to an infantile cortical hyperostosis (Caffey disease), for which SLC37A2 is a new candidate gene. 27187611 2016