AMBN, ameloblastin, 258

N. diseases: 23; N. variants: 1
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C4225394
Disease: AMELOGENESIS IMPERFECTA, TYPE IF
AMELOGENESIS IMPERFECTA, TYPE IF
0.600 Biomarker disease GENOMICS_ENGLAND A targeted next-generation sequencing assay for the molecular diagnosis of genetic disorders with orodental involvement. 26502894 2016
CUI: C4225394
Disease: AMELOGENESIS IMPERFECTA, TYPE IF
AMELOGENESIS IMPERFECTA, TYPE IF
0.600 Biomarker disease CTD_human
CUI: C4225394
Disease: AMELOGENESIS IMPERFECTA, TYPE IF
AMELOGENESIS IMPERFECTA, TYPE IF
0.600 CausalMutation disease CLINVAR