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GENATLAS PHENOTYPE

last update : 27-11-2018

Symbol	ICS41
Location	11p15.5
Name	immotile cilia syndrome 41
Other name(s)	ciliary dyskinesia, primary, 39
Corresponding gene	LRRC56
Other symbol(s)	CILD39
Main clinical features	laterality defects varying from partial to complete situs inversus, associated with bronchiectasis, chronic lung infections, middle ear infection
Genetic determination	autosomal recessive
Function/system disorder	cardiovascular
	ear
	respiratory
Type	disease

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