Disease: Amelogenesis imperfecta and gingival hyperplasia syndrome ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C3873241
Disease: Amelogenesis imperfecta and gingival hyperplasia syndrome
Amelogenesis imperfecta and gingival hyperplasia syndrome 		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
CUI: C3873241
Disease: Amelogenesis imperfecta and gingival hyperplasia syndrome
Amelogenesis imperfecta and gingival hyperplasia syndrome 		0.020 GeneticVariation disease BEFREE Whole-Exome sequencing identifies FAM20A mutations as a cause of amelogenesis imperfecta and gingival hyperplasia syndrome. 21549343 2011