primary ciliary dyskinesia 29 (DOID:0110600)
Alliance: disease page
Synonyms: CILD29; primary ciliary dyskinesia 29 without situs inversus
Alt IDs: OMIM:615872, ICD10CM:Q34.8
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.