Disease: Hypomineralized amelogenesis imperfecta ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C4478871
Disease: Hypomineralized amelogenesis imperfecta
Hypomineralized amelogenesis imperfecta 		0.300 Biomarker phenotype GENOMICS_ENGLAND Screening of a panel of 57 autosomal-recessive AI-affected families identified eight further families with loss-of-function mutations in C4orf26. 22901946 2012