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GENATLAS PHENOTYPE

last update : 12-11-2015

Symbol	ICS6
Location	7p14.1
Name	immotile cilia syndrome 6
Other name(s)	Ciliary dyskinesia, primary, 6
Corresponding gene	NME8
Other symbol(s)	CILD6
Main clinical features	immotile cilia syndrome characterized by chronic respiratory symptoms, ciliary abnormalities in association with recurrent respiratory infections and retinitis pigmentosa
Genetic determination	autosomal recessive
Function/system disorder	defense and immunity
	eye
	respiratory
Type	disease

Remark(s)