MKS1, MKS transition zone complex subunit 1, 54903

N. diseases: 231; N. variants: 57
Disease: Tetralogy of Fallot ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0039685
Disease: Tetralogy of Fallot
Tetralogy of Fallot 		0.210 Biomarker disease MGD Genome-wide identification of mouse congenital heart disease loci. 20511334 2010
CUI: C0039685
Disease: Tetralogy of Fallot
Tetralogy of Fallot 		0.210 GeneticVariation disease BEFREE The dual midline fusion defects of tetralogy of Fallot and MA suggests that either this patient has a unique syndrome with a distinct genetic etiology or that she has a genetically heterogeneous or variant form of MKS. 15266619 2004