Disease-gene associations mined from literature

Human genes for tetralogy of Fallot

Tetralogy of Fallot [DOID:6419]

Tetralogy of Fallot (TOF) is a congenital heart defect which is classically understood to involve four anatomical abnormalities (although only three of them are always present). It is the most common cyanotic heart defect, and the most common cause of blue baby syndrome.

Synonyms:  tetralogy of Fallot,  DOID:6419,  Tetralogy of Fallot (disorder),  Tetralogy of Fallot NOS (disorder),  Tetralogy of Fallot, unspecified ...