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Summary Literature (0)
DOID:0110600 - primary ciliary dyskinesia 29


Disease Ontology 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.

Synonyms: CILD29, primary ciliary dyskinesia 29 without situs inversus

In OMIM:
OMIM:615872 - CILIARY DYSKINESIA, PRIMARY, 29; CILD29

In Mondo Disease Ontology:
MONDO:0014378 - primary ciliary dyskinesia 29

Human Disease Resources: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Xenbase Genes : ccno

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Parent(s): primary ciliary dyskinesia (is_a)