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GENATLAS PHENOTYPE
last update : 04-06-2010
Symbol TARP
Location Xp11.23
Name TARP syndrome
Other name(s) Pierre Robin syndrome with congenital heart malformation and clubfoot
Corresponding gene RBM10
Other symbol(s) TARPS
Main clinical features
  • talipes equinovarus, atrial septal defect, Robin sequence, and persistence of the left superior vena cava
  • Genetic determination sex linked
    Function/system disorder cardiovascular
    congenital malformation
    neurology
    Type disease
    Remark(s)