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GENATLAS PHENOTYPE

last update : 27-02-2013

Symbol	VACTERLX
Location	Xq26.3
Name	X-linked VACTERL syndrome with or without hydrocephalus
Corresponding gene	ZIC3
Main clinical features	radial ray abnormalities, renal anomalies, anal atresia, hypoplastic penis/abnormal testes, and cardiac abnormalities heterotaxy, complex or isolated heart defect as well as other midline urogenital and hindgut malformations
Genetic determination	sex linked
Function/system disorder	cardiovascular
	digestive tract/gastrointestinal
	neurology
	osteo-articular
	kidney and urinary tract
Type	disease

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