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Disease Ontology Browser
primary ciliary dyskinesia 10 (DOID:0110612)
Alliance: disease page
Synonyms: CILD10; primary ciliary dyskinesia 10 with or without situs inversus
Alt IDs: OMIM:612518, ICD10CM:Q34.8
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.

Disease References using Mouse Models (2)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB), Gene Ontology (GO)
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last database update
MGI 6.14
The Jackson Laboratory