Home Page

References

OMIM

Gene

GeneReviews

HGMD

HGNC

GENATLAS PHENOTYPE

last update : 22-11-2016

Symbol	HTX5
Location	10q22.1
Name	heterotaxy, visceral, 5
Corresponding gene	NODAL
Main clinical features	developmental disorder characterized by complex congenital heart malformations and/or situs inversus and caused by defects in the normal left-right asymmetric positioning of internal organs
Genetic determination	not applicable
Function/system disorder	cardiovascular
	digestive tract/gastrointestinal
Type	disease

Remark(s)