Disease: AMELOGENESIS IMPERFECTA, HYPOMATURATION TYPE, IIA4 ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C3553830
Disease: AMELOGENESIS IMPERFECTA, HYPOMATURATION TYPE, IIA4
AMELOGENESIS IMPERFECTA, HYPOMATURATION TYPE, IIA4 		0.600 Biomarker disease GENOMICS_ENGLAND Mutations in C4orf26, encoding a peptide with in vitro hydroxyapatite crystal nucleation and growth activity, cause amelogenesis imperfecta. 22901946 2012
CUI: C3553830
Disease: AMELOGENESIS IMPERFECTA, HYPOMATURATION TYPE, IIA4
AMELOGENESIS IMPERFECTA, HYPOMATURATION TYPE, IIA4 		0.600 Biomarker disease GENOMICS_ENGLAND Mutations in C4orf26, encoding a peptide with in vitro hydroxyapatite crystal nucleation and growth activity, cause amelogenesis imperfecta. 22901946 2012
CUI: C3553830
Disease: AMELOGENESIS IMPERFECTA, HYPOMATURATION TYPE, IIA4
AMELOGENESIS IMPERFECTA, HYPOMATURATION TYPE, IIA4 		0.600 Biomarker disease GENOMICS_ENGLAND
CUI: C3553830
Disease: AMELOGENESIS IMPERFECTA, HYPOMATURATION TYPE, IIA4
AMELOGENESIS IMPERFECTA, HYPOMATURATION TYPE, IIA4 		0.600 Biomarker disease CTD_human
CUI: C3553830
Disease: AMELOGENESIS IMPERFECTA, HYPOMATURATION TYPE, IIA4
AMELOGENESIS IMPERFECTA, HYPOMATURATION TYPE, IIA4 		0.600 CausalMutation disease CLINVAR