Gene: FAM20A ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 54757
Gene Symbol: FAM20A
FAM20A 		0.020 GeneticVariation disease BEFREE Further evidence for causal FAM20A mutations and first case of amelogenesis imperfecta and gingival hyperplasia syndrome in Morocco: a case report. 25636655 2015
Entrez Id: 54757
Gene Symbol: FAM20A
FAM20A 		0.020 GeneticVariation disease BEFREE Whole-Exome sequencing identifies FAM20A mutations as a cause of amelogenesis imperfecta and gingival hyperplasia syndrome. 21549343 2011