Source: ALL

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 8241
Gene Symbol: RBM10
RBM10
CUI: C0009081
Disease: Congenital clubfoot
Congenital clubfoot 		0.120 GeneticVariation BEFREE Mutations in RBM10 are associated with TARP syndrome, an X-linked recessive disorder originally described with cardinal features of talipes equinovarus, atrial septal defect, Robin sequence, and persistent left superior vena cava. 28577551

2017
Entrez Id: 8241
Gene Symbol: RBM10
RBM10
CUI: C0009081
Disease: Congenital clubfoot
Congenital clubfoot 		0.120 Biomarker BEFREE Some genes, including PITX1, TBX4, and RBM10, have been associated with CTEV. 27395407

2016
Entrez Id: 8241
Gene Symbol: RBM10
RBM10
CUI: C0009081
Disease: Congenital clubfoot
Congenital clubfoot 		0.120 Biomarker HPO