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DOID:0110612 - primary ciliary dyskinesia 10
Disease Ontology Definition:A primary ciliary dyskinesia that is characterized by outer and inner dynein arm absence, chronic otitis media, sinusitis, recurrent pneumonia and variable occurrence of situs inversus and has_material_basis_in homozygous mutation in the KTU gene on chromosome 14q21.
Synonyms: CILD10, primary ciliary dyskinesia 10 with or without situs inversus,
Echinobase Genes :
MIM:612518 - ciliary dyskinesia, primary, 10; cild10 |
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
primary ciliary dyskinesia (is_a)