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Disease Ontology Browser
primary ciliary dyskinesia 29 (DOID:0110600)
Synonyms: CILD29; primary ciliary dyskinesia 29 without situs inversus
Alt IDs: OMIM:615872, ICD10CM:Q34.8, ORDO:244
Definition: A primary ciliary dyskinesia that is characterized by autosomal recessive inheritance with oligocilia and early childhood onset of recurrent respiratory infections, and has_material_basis_in homozygous or compound heterozygous mutation in the CCNO gene on chromosome 5p15.


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Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
03/14/2017
MGI 6.08
The Jackson Laboratory