Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 4488
Gene Symbol: MSX2
MSX2 		0.710 Biomarker disease GENOMICS_ENGLAND Second family with the Boston-type craniosynostosis syndrome: novel mutation and expansion of the clinical spectrum. 23918290 2013
Entrez Id: 4488
Gene Symbol: MSX2
MSX2 		0.710 Biomarker disease GENOMICS_ENGLAND PFMCCD is indeed aetiologically distinct from CCD, which is caused by mutations in the RUNX2 gene, but allelic with isolated PFM, in which MSX2 mutations were previously identified. 14571277 2003
Entrez Id: 4488
Gene Symbol: MSX2
MSX2 		0.710 GeneticVariation disease BEFREE Parietal foramina with cleidocranial dysplasia is caused by mutation in MSX2. 14571277 2003
Entrez Id: 4488
Gene Symbol: MSX2
MSX2 		0.710 Biomarker disease GENOMICS_ENGLAND
Entrez Id: 4488
Gene Symbol: MSX2
MSX2 		0.710 GermlineCausalMutation disease ORPHANET
Entrez Id: 4488
Gene Symbol: MSX2
MSX2 		0.710 CausalMutation disease CLINVAR
Entrez Id: 4488
Gene Symbol: MSX2
MSX2 		0.710 Biomarker disease CTD_human