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GENATLAS PHENOTYPE

last update : 23-11-2013

Symbol	ICS26
Location	15q21.3
Name	immotile cilia syndrome 26
Other name(s)	Ciliary dyskinesia, primary, 25
Corresponding gene	DYX1C1
Other symbol(s)	CILD25
Main clinical features	defective ciliary movement; recurrent upper and lower airway disease, bronchiectasis, and decreased fertility about half of patients show laterality defects, including situs inversus totalis. respiratory cilia from patients show defects in the inner and outer dynein arm
Genetic determination	autosomal recessive
Function/system disorder	defense and immunity
Type	disease

Remark(s)