primary ciliary dyskinesia 10

Summary

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

Xenbase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: dnaaf2

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0012918 - primary ciliary dyskinesia 10

MONDO:0012918 - primary ciliary dyskinesia 10

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): primary ciliary dyskinesia (is_a)