Source: CTD_human

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 286077
Gene Symbol: FAM83H
FAM83H
CUI: C0376634
Disease: Craniofacial Abnormalities
Craniofacial Abnormalities 		0.300 Biomarker CTD_human Phenotypic variation in FAM83H-associated amelogenesis imperfecta. 19407157

2009