ciliary dyskinesia Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A deviation from the normally well coordinated pattern of intracellular and intercellular synchrony of motile cilia. Dyskinetic cilia usually beat out of synchrony relative to neighboring cilia. (Human Phenotype Ontology, HP_0012265)
External Link
Similar Terms
Downloads & Tools


4 genes associated with the ciliary dyskinesia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
CCDC103 coiled-coil domain containing 103
CCDC114 coiled-coil domain containing 114
HYDIN HYDIN, axonemal central pair apparatus protein
RSPH9 radial spoke head 9 homolog (Chlamydomonas)