Disease-gene associations mined from literature

Human genes for primary ciliary dyskinesia

Primary ciliary dyskinesia [DOID:9562]

An autosomal recessive genetic disease that causes a defect in the action of the cilia lining the respiratory tract (lower and upper, sinuses, Eustachian tube, middle ear) and fallopian tube.

Synonyms:  primary ciliary dyskinesia,  DOID:9562,  cliary motility disorder,  immotile ciliary syndrome,  cliary motility disease ...