ICD-11 code : CB40.0;
Preferred Label : Ciliary dyskinesia;
ICD-11 definition : Defective function of the cilia lining the respiratory tract (lower and upper, sinuses,
Eustachian tube, middle ear) resulting in altered mucociliary transport and manifesting
as recurrent upper and lower respiratory infection, chronic productive cough, chronic
rhinosinusitis or persistent otitis media. Acquired forms result from respiratory
tract injury associated especially with respiratory infections such as bronchiolitis
or chronic obstructive pulmonary disease. The rare primary forms are inherited as
autosomal recessive disorders presenting early in life and typically progressing to
bronchiectasis; they may be associated with infertility in men and women due to abnormal
sperm motility or fallopian tube function respectively.;
Origin ID : 955573234;
Currated CISMeF NLP mapping
- Validated automatic mappings to NTBT
Defective function of the cilia lining the respiratory tract (lower and upper, sinuses,
Eustachian tube, middle ear) resulting in altered mucociliary transport and manifesting
as recurrent upper and lower respiratory infection, chronic productive cough, chronic
rhinosinusitis or persistent otitis media. Acquired forms result from respiratory
tract injury associated especially with respiratory infections such as bronchiolitis
or chronic obstructive pulmonary disease. The rare primary forms are inherited as
autosomal recessive disorders presenting early in life and typically progressing to
bronchiectasis; they may be associated with infertility in men and women due to abnormal
sperm motility or fallopian tube function respectively.
