Disease: Hypodontia ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0020608
Disease: Hypodontia
Hypodontia 		0.110 GeneticVariation disease BEFREE Mutation of KREMEN1, a modulator of Wnt signaling, is responsible for ectodermal dysplasia including oligodontia in Palestinian families. 27049303 2016
CUI: C0020608
Disease: Hypodontia
Hypodontia 		0.110 Biomarker disease HPO