Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 3239
Gene Symbol: HOXD13
HOXD13 		0.700 Biomarker disease CTD_human Human HOX gene disorders. 24239177 2014
Entrez Id: 3239
Gene Symbol: HOXD13
HOXD13 		0.700 Biomarker disease GENOMICS_ENGLAND Mutations in HOXD13 underlie syndactyly type V and a novel brachydactyly-syndactyly syndrome. 17236141 2007
Entrez Id: 3239
Gene Symbol: HOXD13
HOXD13 		0.700 GeneticVariation disease UNIPROT Missense mutations in the homeodomain of HOXD13 are associated with brachydactyly types D and E. 12649808 2003
Entrez Id: 3239
Gene Symbol: HOXD13
HOXD13 		0.700 Biomarker disease GENOMICS_ENGLAND Missense mutations in the homeodomain of HOXD13 are associated with brachydactyly types D and E. 12649808 2003
Entrez Id: 3239
Gene Symbol: HOXD13
HOXD13 		0.700 Biomarker disease GENOMICS_ENGLAND
Entrez Id: 3239
Gene Symbol: HOXD13
HOXD13 		0.700 CausalMutation disease CLINVAR
Entrez Id: 3239
Gene Symbol: HOXD13
HOXD13 		0.700 Biomarker disease HPO
Entrez Id: 2047
Gene Symbol: EPHB1
EPHB1 		0.010 Biomarker disease BEFREE The results suggest that BDD-NET can be safely and effectively delivered across international borders to a culturally diverse sample. 30904854 2019
Entrez Id: 2004
Gene Symbol: ELK3
ELK3 		0.010 Biomarker disease BEFREE The results suggest that BDD-NET can be safely and effectively delivered across international borders to a culturally diverse sample. 30904854 2019
Entrez Id: 6530
Gene Symbol: SLC6A2
SLC6A2 		0.010 Biomarker disease BEFREE The results suggest that BDD-NET can be safely and effectively delivered across international borders to a culturally diverse sample. 30904854 2019
Entrez Id: 3596
Gene Symbol: IL13
IL13 		0.010 AlteredExpression disease BEFREE Before acute-phase treatment, the initial levels of TNF-α and IL-13 were significantly lower in the BDD patients than in the MDD patients. 29778935 2018
Entrez Id: 1401
Gene Symbol: CRP
CRP 		0.010 Biomarker disease BEFREE Baseline CRP levels were significantly increased amongst BDD patients versus HC subjects, indicating that CRP may be a useful biomarker for BDD (P = 0.044). 29554535 2018
Entrez Id: 3198
Gene Symbol: HOXA1
HOXA1 		0.010 GeneticVariation disease BEFREE This is the first study to report significant linkage results for BDD/BDE using a large extended pedigree, and the first to suggest that mutations in TWIST and/or the HOXA1-A13 cluster may contribute to these specific skeletal anomalies. 24022874 2014
Entrez Id: 7291
Gene Symbol: TWIST1
TWIST1 		0.010 GeneticVariation disease BEFREE This is the first study to report significant linkage results for BDD/BDE using a large extended pedigree, and the first to suggest that mutations in TWIST and/or the HOXA1-A13 cluster may contribute to these specific skeletal anomalies. 24022874 2014