Disease: ECTODERMAL DYSPLASIA 13, HAIR/TOOTH TYPE ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C4479322
Disease: ECTODERMAL DYSPLASIA 13, HAIR/TOOTH TYPE
ECTODERMAL DYSPLASIA 13, HAIR/TOOTH TYPE 		0.600 Biomarker disease GENOMICS_ENGLAND Mutation of KREMEN1, a modulator of Wnt signaling, is responsible for ectodermal dysplasia including oligodontia in Palestinian families. 27049303 2016
CUI: C4479322
Disease: ECTODERMAL DYSPLASIA 13, HAIR/TOOTH TYPE
ECTODERMAL DYSPLASIA 13, HAIR/TOOTH TYPE 		0.600 GeneticVariation disease UNIPROT Mutation of KREMEN1, a modulator of Wnt signaling, is responsible for ectodermal dysplasia including oligodontia in Palestinian families. 27049303 2016
CUI: C4479322
Disease: ECTODERMAL DYSPLASIA 13, HAIR/TOOTH TYPE
ECTODERMAL DYSPLASIA 13, HAIR/TOOTH TYPE 		0.600 Biomarker disease CTD_human