TNNT3, troponin T3, fast skeletal type, 7140

N. diseases: 52; N. variants: 4
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 		0.110 GeneticVariation disease BEFREE Although mutations in MYH3, TNNT3, and TPM2 are frequently associated with distal arthrogryposis syndromes, they were not present in patients with familial vertical talus or clubfoot. 19142688 2009
CUI: C0009081
Disease: Congenital clubfoot
Congenital clubfoot 		0.110 Biomarker disease HPO