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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
    Remark(s)