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 http://compbio.charite.de/hpoweb/showterm?id=HP:0012265
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Genes

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)