Disease: Amelogenesis imperfecta nephrocalcinosis ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C2931783
Disease: Amelogenesis imperfecta nephrocalcinosis
Amelogenesis imperfecta nephrocalcinosis 		0.010 GeneticVariation disease BEFREE The purpose of this study was to search for novel KCND3 mutations associated with ERS and to clarify the pathogenesis. 31173922 2019