Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0036439
Disease: Scoliosis, unspecified
Scoliosis, unspecified
0.410 Biomarker disease CTD_human Thus, Dll3-Notch1 double heterozygous mice model human congenital scoliosis and craniofacial disorders. 17849441 2007
CUI: C0036439
Disease: Scoliosis, unspecified
Scoliosis, unspecified
0.410 GeneticVariation disease BEFREE Scoliosis has been observed in a heterozygous DLL3 carrier, raising the possibility of its involvement in congenital scoliosis. 15717203 2005
CUI: C0036439
Disease: Scoliosis, unspecified
Scoliosis, unspecified
0.410 Biomarker disease HPO