RBM10, RNA binding motif protein 10, 8241

N. diseases: 99; N. variants: 8
Disease: Congenital clubfoot ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0009081
Disease: Congenital clubfoot
Congenital clubfoot 		0.120 GeneticVariation disease 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
CUI: C0009081
Disease: Congenital clubfoot
Congenital clubfoot 		0.120 Biomarker disease BEFREE Some genes, including PITX1, TBX4, and RBM10, have been associated with CTEV. 27395407 2016
CUI: C0009081
Disease: Congenital clubfoot
Congenital clubfoot 		0.120 Biomarker disease HPO