Gene: EDN1 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 1906
Gene Symbol: EDN1
EDN1 		0.610 GeneticVariation disease BEFREE Auriculocondylar syndrome and isolated question mark ear result from dysregulation of the endothelin 1-endothelin receptor type A signaling pathway. 28456137 2018
Entrez Id: 1906
Gene Symbol: EDN1
EDN1 		0.610 Biomarker disease GENOMICS_ENGLAND Mutations in endothelin 1 cause recessive auriculocondylar syndrome and dominant isolated question-mark ears. 24268655 2013
Entrez Id: 1906
Gene Symbol: EDN1
EDN1 		0.610 Biomarker disease HPO
Entrez Id: 1906
Gene Symbol: EDN1
EDN1 		0.610 Biomarker disease CTD_human