AMBN, ameloblastin, 258

N. diseases: 23; N. variants: 1
Disease: Amelogenesis Imperfecta, Type IB ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0399368
Disease: Amelogenesis Imperfecta, Type IB
Amelogenesis Imperfecta, Type IB 		0.010 Biomarker disease BEFREE This study excludes the coding regions and the splice sites of AMBN from a causative role in the pathogenesis of AIH2. 11330937 2001