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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

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