Human genes for primary ciliary dyskinesia
Primary ciliary dyskinesia [DOID:9562]
A ciliopathy that is characterized by impaired function of the cilia lining the respiratory tract (lower and upper, sinuses, Eustachian tube, middle ear) and fallopian tube.
Synonyms: primary ciliary dyskinesia, DOID:9562, primary ciliary dyskinesias, ciliary motility disorder, immotile ciliary syndrome ...
Linkouts: OMIM #1 #2 #3 #4 #5 #6 #7 #8 #9 #10 #11 #12 #13 #14 #15 #16 #17 #18 #19 #20