MSX1, msh homeobox 1, 4487

N. diseases: 180; N. variants: 21
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1837210
Disease: OROFACIAL CLEFT 5
OROFACIAL CLEFT 5
0.700 Biomarker disease GENOMICS_ENGLAND Mutations in the MSX1 gene in Turkish children with non-syndromic tooth agenesis and other dental anomalies. 25565750 2014
CUI: C1837210
Disease: OROFACIAL CLEFT 5
OROFACIAL CLEFT 5
0.700 Biomarker disease GENOMICS_ENGLAND In a Vietnamese population, MSX1 variants contribute to cleft lip and palate. 15354328 2005
CUI: C1837210
Disease: OROFACIAL CLEFT 5
OROFACIAL CLEFT 5
0.700 GeneticVariation disease UNIPROT Complete sequencing shows a role for MSX1 in non-syndromic cleft lip and palate. 12807959 2003
CUI: C1837210
Disease: OROFACIAL CLEFT 5
OROFACIAL CLEFT 5
0.700 Biomarker disease GENOMICS_ENGLAND
CUI: C1837210
Disease: OROFACIAL CLEFT 5
OROFACIAL CLEFT 5
0.700 CausalMutation disease CLINVAR
CUI: C1837210
Disease: OROFACIAL CLEFT 5
OROFACIAL CLEFT 5
0.700 Biomarker disease CTD_human