Source: ALL

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 1055
Gene Symbol: CECR
CECR
CUI: C0376634
Disease: Craniofacial Abnormalities
Craniofacial Abnormalities 		0.300 Biomarker CTD_human Phenotypic variability of the cat eye syndrome. Case report and review of the literature. 11693792

2001